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Symptoms » Reading symptoms » Glossary
 

Glossary for Reading symptoms

Medical terms related to Reading symptoms or mentioned in this section include:

  • 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
  • Aphasia: inability to produce and comprehend language
  • Apraxia, oculomotor, Cogan type: A rare inherited condition where the person is unable to move eyes horizontally making it difficult to follow objects.
  • Auditory perceptual disorder: A hearing disorder where the brain is unable to properly process or interpret auditory information it receives from the hearing organs.
  • 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
  • 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.
  • 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.
  • Developmental problems: Physical or mental development difficulty.
  • 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..
  • 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.
  • Head symptoms: Symptoms affecting the head or brain
  • Hyperopia: Inability to focus on close objects.
  • Infant symptoms: Symptoms affecting babies and infants.
  • 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.
  • Language problems: Symptoms affecting language processing.
  • 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: Melanoma is the most dangerous type of skin cancer. It is the leading cause of death from skin disease. It involves cells called melanocytes, which produce a skin pigment called melanin. Melanin is responsible for skin and hair color.
  • 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.
  • 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.
  • Presbyopia: Age-related far-sightedness often requiring glasses
  • 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.
  • 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.
  • School problems: Difficulty with learning or schooling as a symptom.
  • 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-like aphasia: Inability to produce and comprehend language.
  • 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: Reading symptoms:

The following list of conditions have 'Reading symptoms' 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.

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Conditions listing medical complications: Reading symptoms:

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

 

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