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Symptoms » Language problems » Glossary
 

Glossary for Language problems

Medical terms related to Language problems or mentioned in this section include:

  • 47 XYY syndrome: A genetic condition where males have an extra Y chromosome in each of their cells. Normally male cells have one X and one Y chromosome. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomatic.
  • 47,XXX syndrome: A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomatic.
  • Aging: The medical conditions from getting older.
  • Alopecia -- hypogonadism -- extrapyramidal disorder: A rare syndrome characterized by alopecia, progressive movement problems and a lack of gonadal function which affects puberty.
  • Alzheimer disease 10: An inherited form of Alzheimer's. Type 10 is caused by a genetic defect on chromosome 10p13.
  • Alzheimer disease 12: An inherited form of Alzheimer's. Type 12 is caused by a genetic defect on chromosome 8p12-q22.
  • Alzheimer disease 13: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 1q21. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 14: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 1q25. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 15: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 3q22-q24. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 16: Alzheimer disease 16 (late-onset) is a form of Alzheimer's disease that is linked to a defect on chromosome Xq21.3. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 2, late-onset: Alzheimer disease 2 (late-onset) is a form of Alzheimer's disease that is linked to a defect on chromosome 19q13.2. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 3, (early-onset Alzheimer disease): Alzheimer disease 3 is an early-onset form of Alzheimer's disease that is linked to a defect on chromosome 14q24.3. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 5: An inherited form of Alzheimer's. Type 5 has a late onset and is caused by a genetic defect on chromosome 12p11.
  • Alzheimer disease 6: A genetic form of Alzheimer's. Type 6 has a late onset and is caused by a genetic defect on chromosome 10q24.
  • Alzheimer disease 7: An inherited form of Alzheimer's. Type 7 is caused by a genetic defect on chromosome 10p13.
  • Alzheimer disease 8: An inherited form of Alzheimer's. Type 8 is caused by a genetic defect on chromosome 20p.
  • Alzheimer disease 9: A genetic form of Alzheimer's. Type 9 has a late onset and is caused by a genetic defect on chromosome 19p13.2.
  • Alzheimer disease, early-onset, with cerebral amyloid angiopathy: An early-onset form of Alzheimer's disease that is linked to a defect on chromosome 21q21. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 1: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 21q. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 11: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 9p22.1. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 3, with spastic paraparesis and apraxia: This form of Alzheimer's is an early-onset form of Alzheimer's that is linked to a defect on chromosome 14q24.3. It is characterized by features which are atypical for Alzheimer's - spastic paraparesis which occurs before the dementia symptoms and apraxia. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques: This form of Alzheimer's is an early-onset form of Alzheimer's that is linked to a defect on chromosome 14q24.3. It is characterized by features which are atypical for Alzheimer's - spastic paraparesis which occurs before the dementia symptoms and unusual plaques in the brain. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 4: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 1q31-q42. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer's disease: A progressive degenerative disease of the brain of unknown cause
  • Angelman syndrome: A rare genetic disorder characterized by a puppet-like gait, fits of laughter and characteristic facial features.
  • Aphasia: inability to produce and comprehend language
  • Apraxia: A disorder of skilled movement not due to tremors, weakness, akinesia or abnormal tone or posture.
  • Apraxia, oculomotor, Cogan type: A rare inherited condition where the person is unable to move eyes horizontally making it difficult to follow objects.
  • Asperger Syndrome, Susceptibility to, 1: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. Type 1 is linked to a defect on chromosome 3q25-q27.
  • Asperger Syndrome, Susceptibility to, 2: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. Type 2 is linked to a defect on chromosome 17p13.
  • Asperger Syndrome, Susceptibility to, 3: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. Type 3 is linked to a defect on chromosome 1q21-q22.
  • Asperger Syndrome, X-linked, Susceptibility to, 1: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. X-linked type 1 is linked to a defect on chromosome Xq13.
  • Asperger Syndrome, X-linked, Susceptibility to, 2: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. X-linked type 1 is linked to a defect on chromosome Xp22.3.
  • Asperger syndrome: A neuropsychiatric disorder mainly involving the inability to understand and becoming involved in social interaction.
  • Auditory perceptual disorder: A hearing disorder where the brain is unable to properly process or interpret auditory information it receives from the hearing organs.
  • Autism: Childhood mental condition with social and communication difficulties.
  • Autism, Susceptibility to, 15: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 15 is linked to a genetic defect on chromosome 7q35-q36.
  • Autism, X-linked, susceptibility to, 1: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. X-Linked type 1 is linked to a genetic defect on chromosome Xq13.
  • Autism, X-linked, susceptibility to, 2: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. X-Linked type 2 is linked to a genetic defect on chromosome Xp22.3.
  • Autism, X-linked, susceptibility to, 3: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. X-Linked type 3 is linked to a genetic defect on chromosome Xp22.3.
  • Autism, susceptibility to, 1: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 1 is linked to a genetic defect on chromosome 7q22.
  • Autism, susceptibility to, 10: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 10 is linked to a genetic defect on chromosome 7q36.
  • Autism, susceptibility to, 11: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 11 is linked to a genetic defect on chromosome 1q24.
  • Autism, susceptibility to, 12: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 12 is linked to a genetic defect on chromosome 21p13-q11.
  • Autism, susceptibility to, 13: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 13 is linked to a genetic defect on chromosome 12q14.
  • Autism, susceptibility to, 14: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 14 is linked to a genetic defect on chromosome 16p11.2.
  • Autism, susceptibility to, 3: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 3 is linked to a genetic defect on chromosome 13q14.
  • Autism, susceptibility to, 4: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 4 is linked to a genetic defect on chromosome 15q11.
  • Autism, susceptibility to, 5: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 5 is linked to a genetic defect on chromosome 2q.
  • Autism, susceptibility to, 6: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 6 is linked to a genetic defect on chromosome 17q11.
  • Autism, susceptibility to, 7: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 7 is linked to a genetic defect on chromosome 17q21.
  • Autism, susceptibility to, 8: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 8 is linked to a genetic defect on chromosome 3q25-q27.
  • Autism, susceptibility to, 9: A developmental disorder characterized by an impaired ability to communicate with or relate to people or the environment around them and repetitive behavior. The severity of the disorder is variable. Researchers have discovered a number of genetic abnormalities linked to an increased susceptibility of developing autism. Type 9 is linked to a genetic defect on chromosome 7q31.
  • Behavioral symptoms: Symptoms of personal behavior.
  • Benign Fasciculation Syndrome: Common movement disorder manifesting in a fine (fast) tremor; it is an inherited condition of unknown cause.
  • Brain symptoms: Symptoms affecting the brain
  • Catatonic syndrome: A rare syndrome often seen in schizophrenics or associated with central nervous system disturbances or brain trauma. The symptoms tend to occur in episodes with periods of remission in between.
  • Child health symptoms: Symptoms related to pediatric (child) health.
  • Childhood-onset cerebral X-linked adrenoleukodystrophy: A rare genetic disorder characterized by progressive degeneration of the protective sheath around nerves resulting in increasing difficulty. The childhood cerebral form of the condition is the most severe.
  • Chromosome 15 inverted duplication: A rare chromosomal disorder involving an duplicated section of chromosome 15 which is reversed end-to-end resulting in various abnormalities.
  • Chromosome 22q11 Deletion Spectrum: A rare chromosomal disorder where a small piece of genetic material is missing from chromosome 22 at the q11 location.
  • Cognitive impairment: General loss of mental or cognitive ability
  • Communication symptoms: Symptoms related to problems with communication.
  • Congenital X-linked retinoschisis: An inherited eye condition where degenerative changes in the eye causes the retina to split. The severity and age of onset of symptoms can vary.
  • Continuous spike-wave during slow sleep syndrome: A rare form of epilepsy that occurs between the ages of 3 and 7 and is diagnosed by the observation through an EEG of continuous spike and wave discharges during the slow sleep phase which is detected. The seizures often occur during sleep. Children outgrow the condition before adulthood but some of the effects of the disorder may continue longer.
  • Deletion 22q11: A rare chromosomal disorder where a small piece of genetic material is missing from chromosome 22 at the q11 location.
  • Developmental problems: Physical or mental development difficulty.
  • DiGeorge syndrome: 22q11.2 deletion syndrome is a genetic disorder which can result in a vast array of symptoms. Various names have been used to describe different manifestations of the syndrome. Di George Syndrome primarily involves an underdeveloped thymus and parathyroid glands which results in lowered immunity low blood calcium levels respectively. Another primary feature is heart defects. Various other variable features are also present. It is not uncommon for patients to have more than one of the 22q11.2 deletion syndrome subtypes which can make diagnosis confusing - other subtypes include Sphrintzen syndrome, Caylor cardiofacial syndrome and CATCH 22.
  • Down's Syndrome associated Alzheimer's disease: Early-onset Alzheimer's is more prevalent in Down's Syndrome sufferers than in the general population. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Dysgraphia: Impaired writing ability due to a pathological disorder.
  • Dyslexia: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia.
  • Dyslexia, Susceptibility to, 1: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 1 is linked to a defect on chromosome 15q21.
  • Dyslexia, Susceptibility to, 2: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 2 is linked to a defect on chromosome 6p22.2.
  • Dyslexia, Susceptibility to, 3: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 3 is linked to a defect on chromosome 2p16-p15.
  • Dyslexia, Susceptibility to, 4: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 4 is linked to a defect on chromosome 6q11.2-q12.
  • Dyslexia, Susceptibility to, 5: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 5 is linked to a defect on chromosome 3p12-q13.
  • Dyslexia, Susceptibility to, 6: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 6 is linked to a defect on chromosome 18p11.2.
  • Dyslexia, Susceptibility to, 7: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 7 is linked to a defect on chromosome 11p15.5.
  • Dyslexia, Susceptibility to, 8: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 8 is linked to a defect on chromosome 1p36-p34.
  • Dyslexia, Susceptibility to, 9: Dyslexia is a name for a condition where people have difficulty with reading and writing. People with dyslexia have normal intelligence and are not in any way mentally retarded or intellectually challenged. The difficulty with certain tasks is believed to be related to problems with perception capability in certain parts of the brain. Researchers have discovered that there are a number of genes linked to an increased susceptibility to dyslexia. Genetic forms of dyslexia are considered to be primary dyslexia and patients tend to have problems with reading, writing and spelling even as adults. Type 9 is linked to a defect on chromosome Xq27.3.
  • Dystonia: Dystonia is a neurological disorder that causes involuntary contractions of muscles in a repetitive, twisting manner.
  • Early-onset Alzheimer's: Early-onset Alzheimer's is a form of Alzheimer's disease that is linked to genetic defects or occurs in a familial pattern. It is not as common as the non-inherited form of Alzheimer's - occurs in up to 90% of Alzheimer sufferers. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Familial Forms of Alzheimer's Disease: Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour. Familial forms of the disease tend to run in families and are linked to mutations on various genes. Chromosome 1, 14 19 and 21 are the main chromosomes where mutations resulting in Alzheimer's are located..
  • Frontotemporal dementia: A degenerative brain disease involving frontal and temporal brain lobes resulting in dementia. Degeneration of the frontal lobe causes behavioral and personality changes degeneration of the temporal lobe causes semantic dementia.
  • Frontotemporal dementia, ubiquitin-positive: A rare inherited neurodegenerative disorder characterized primarily by progressive social, behavioral and language deterioration due to changes in the frontotemporal portion of the brain.
  • Gerstmann's Syndrome: Brain defect causing various cognitive problems.
  • Glioma: A rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor.
  • Glioma Susceptibility: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. There have been at least 8 genetic defects linked to an increased glioma susceptibility.
  • Glioma Susceptibility 1: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. Type 1 is linked to a genetic defect on chromosome 3p25.
  • Glioma Susceptibility 2: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. Type 2 is linked to a genetic defect on chromosome 10q23.31.
  • Glioma Susceptibility 3: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. Type 3 is linked to a genetic defect on chromosome 13q12.3.
  • Glioma Susceptibility 4: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. Type 4 is linked to a genetic defect on chromosome 15q23-q26.3.
  • Glioma Susceptibility 5: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. Type 5 is linked to a genetic defect on chromosome 9p21.3.
  • Glioma Susceptibility 6: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. Type 6 is linked to a genetic defect on chromosome 20q13.33.
  • Glioma Susceptibility 7: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. Type 7 is linked to a genetic defect on chromosome 8q24.21.
  • Glioma Susceptibility 8: A glioma is a rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor. Some people have particular genetic anomalies which makes them more susceptible to developing a glioma. Type 8 is linked to a genetic defect on chromosome 5p15.33.
  • Global developmental delay -- osteopenia -- ectodermal defect: A rare syndrome characterized by developmental delay, osteopenia and skin anomalies.
  • Head symptoms: Symptoms affecting the head or brain
  • Hyperopia: Inability to focus on close objects.
  • Inborn amino acid metabolism disorder: A group of inherited disorders where the body is not able to metabolize amino acids consumed in the diet. Amino acids are a part of carbohydrates, fats and proteins and are metabolized in order to provide energy or to make other needed compounds. There are many steps involved in metabolism and the severity can be greatly variable depending on the exact nature of the disorder.
  • Infant symptoms: Symptoms affecting babies and infants.
  • Jumping Frenchmen of Maine: A rare condition where the startle reflex is greatly exaggerated. The startle reflex in this order is characterized by jumping, raising the arms, yelling, hitting, obeying sudden commands and repeating sentences.
  • Juvenile Retinoschisis: An inherited eye condition where degenerative changes in the eye causes the retina to split. The severity and age of onset of symptoms can vary.
  • Juvenile pilocytic astrocytoma: A type of brain tumor that occurs in children and young adults. The tumor is derived from a type of cell called an astrocyte and it can occur in various parts of the brain as well as the optic pathways and the spinal cord. Malignancy is rare. Symptoms may vary depending on the size and location of the tumor.
  • Klinefelter syndrome: A genetic condition where males have at least one extra X chromosome or extra copies of both the X and Y chromosomes in each cell. Normally male cells contain one X and one Y chromosome in each cell. The condition is not inherited but is a result of problems during cell division. Klinefelter syndrome variants is a more severe form of the condition as it involves more than one extra X or X and Y chromosome in each cell.
  • Late-onset Alzheimer's: Late-onset Alzheimer's is a form of Alzheimer's disease that doesn't appear to be linked to any genetic defects or familial pattern. It is by far the most common form of Alzheimer's - occurs in up to 90% of Alzheimer sufferers. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Learning disabilities: Difficulty with learning or schooling.
  • Melanoma -- astrocytoma syndrome: A rare syndrome characterized by the association of a melanoma with a type of brain tumor called an astrocytoma. The exact symptoms may vary depending on the exact location of the brain tumor.
  • Mental problems: Symptoms affecting judgement, thought or intelligence.
  • Mental retardation, X-linked, 16: A rare form of mental retardation inherited in a X-linked manner. It occurs as a result of a defect in the MECP2 gene on chromosome Xq28. Females tended to be affected as well as males although to a lesser degree.
  • Myoclonic epilepsy benign, adult, familial: A rare familial disorder characterized by muscle jerking and seizures in adults. The disorder is not progressive and is fairly harmless with only minor fine motor control problems.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurological symptoms: Any symptoms that are caused by neurological conditions
  • Personality symptoms: Symptoms or changes to the personality.
  • Pervasive developmental disorder: Pervasive developmental disorder refers to a disorder in which there is a delay or lack of development in the ability to communicate or socialize.
  • Pick's disease of the brain: A degenerative brain disease involving the frontal and temporal brain lobes resulting primarily in progressive dementia and loss of motor and language functions. It is characterized by the presence of proteins called Pick bodies in damaged nerve cells.
  • Presbyopia: Age-related far-sightedness often requiring glasses
  • Reading symptoms: Problems with reading ability
  • Retinoschisis: A rare inherited or acquired condition where the retina separates into two layers resulting in progressive vision loss.
  • Retinoschisis, Juvenile, X-Linked: An inherited eye condition where degenerative changes in the eye causes the retina to split. The severity and age of onset of symptoms can vary.
  • Retinoschisis, X-linked: A rare congenital eye disorder inherited in a X-linked manner. It is characterized by the separation of the retina into two layers which results in progressive vision loss. Though close examination may show signs of the condition, symptoms such as noticeable vision impairment generally don't become evident until middle age.
  • Retinoschisis, juvenile: An inherited eye condition where degenerative changes in the eye causes the retina to split. The severity and age of onset of symptoms can vary.
  • Rett's syndrome: Autism-like behavioral syndrome in infant girls
  • Right parietal lobe syndrome related Alzheimer's disease: Right parietal lobe syndrome related Alzheimer's disease is a variant of Alzheimer's disease that involves abnormalities in a particular part of the brain. It is characterized by Alzheimer's symptoms as well as problems with such things as construction (making things) and drawing as well as denial of their disabilities. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Rocky Mountain spotted fever: A bacterial disease caused by Rickettsia rickettsii and transmitted by ticks. The condition causes fever and a characteristic rash and may be fatal in severe or untreated cases.
  • Schizencephaly: A very rare disorder where the brain fails to develop normally and slits or clefts form in the brain. They type and severity of symptoms is determined by the degree of abnormality.
  • School problems: Difficulty with learning or schooling as a symptom.
  • Shprintzen syndorme: An inherited syndrome of cardiac defects and craniofacial anomalies and various other abnormalities.
  • Soto's Syndrome: A rare hereditary disorder characterized by excessive growth during the first few years of life as well as various other mental and physical anomalies.
  • Speech symptoms: Problems with speech or voice.
  • Spinocerebellar ataxia, autosomal recessive 4: A rare neurological disorder caused by a genetic defect (chromosome 1p36, recessive) and resulting in ataxia and eye movement problems.
  • Spinocerebellar ataxia, autosomal recessive 7: A rare, recessively inherited neurological disorder caused by abnormalities in the cerebellum and spinal cord. The severity of the disorder is variable.
  • Stroke symptoms: Brain-related symptoms of bleeding or blockage.
  • Stroke-like aphasia: Inability to produce and comprehend language.
  • Telencephalic leukoencephalopathy: Neurological disease of the brain where the protective sheaths covering the nerves in the brains are destroyed or fail to develop properly.
  • Velocardiofacial syndrome: A genetic disorder which can present with a wide range of phenotypic manifestations which has lead to a number of different names being assigned to the various presentations e.g. DiGeorge Syndrome and Cayler Anomaly Face Syndrome. There are nearly 200 different symptoms that can occur and the severity of the condition is also highly variable depending on the nature and severity of the symptoms that are present.
  • Wilson's disease: Wilson disease, or hepatolenticular degeneration, is a neurodegenerative disease of copper metabolism.
  • Writer's cramp: A condition which is characterized by cramping of the intrinsic muscles of the hand due to use
  • Writing symptoms: Problems with writing ability
  • Zonular cataract and nystagmus: Cataracts that affect only certain layers of the lens

Conditions listing medical symptoms: Language problems:

The following list of conditions have 'Language problems' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

Select from the following alphabetical view of conditions which include a symptom of Language problems or choose View All.

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Conditions listing medical complications: Language problems:

The following list of medical conditions have 'Language problems' or similar listed as a medical complication in our database.

 

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