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Symptoms » Detachment » Glossary
 

Glossary for Detachment

Medical terms related to Detachment or mentioned in this section include:

  • Acanthamoeba infection: Infection with a microscopic, free-living ameba that is readily found in the environment - soil, air and water. Most people exposed to the ameba will not become infected but when infections do occur, they tend to affect the eyes, central nervous system or can cause widespread infection throughout the body.
  • Acanthamoeba infection of the central nervous system: Infection by an amoebic organism called Acanthamoeba. Infection usually occurs when the amoeba enters through a break in the skin or through the nose. Infection can be localized or systemic where it can involve the central nervous system and cause potentially fatal meningoencephalitis. Infection of the eye can occur by cleaning contact lenses in contaminated water.
  • Acute meningitis: Acute meningitis is an inflammation of the brain that presents in an acute fashion. The inflammation may be the result of infective agents such as bacteria, viruses and fungi as well as non-infective agents such as certain drugs. Acute forms of meningitis can develop in within hours or days whereas chronic meningitis develops over weeks or months.
  • Adolescent depression: It isnot unusual for young people to experience "the blues" or feel low occasionally. Adolescence is always an unsettling time, with the many physical, emotional, psychological and social changes that accompany this stage of life.
  • Adrenal hyperplasia: A group of disorder that occur when there is a problem in the process of making adrenal corticosteroids.
  • Adrenal hyperplasia, congenital type 3: A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency.
  • Akinetic mutism: Damage to parts of the brain (e.g. demyelinization and hydrocephalus) which results in a person being unable to talk or move despite the fact that they appear alert at times.
  • 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
  • Amotivational syndrome: An impaired desire to engage in normal social activities and situations due to external factors such as relationships, substance or events.
  • Apathy: When an individual has a lack of feeling and emotion
  • Asperger syndrome: A neuropsychiatric disorder mainly involving the inability to understand and becoming involved in social interaction.
  • Autism: Childhood mental condition with social and communication difficulties.
  • Bacterial meningitis: Bacterial meningitis is a form of meningitis caused by bacteria that normally lives in the mouth and throat. When the immune system is unable to supress this bacteria, it travels to the cerebrospinal spinal fluid in the brain. From there it affects the membranes surrounding the brain.
  • Behavioral symptoms: Symptoms of personal behavior.
  • Bipolar disorder: Cycles of mania and depression; commonly called "manic-depression".
  • Burnout syndrome: Severe stress caused by work-related physical or mental trauma.
  • Chagas disease: A parasitic infection caused by the protozoa Trypanosoma cruzi and transmitted by insect bites or blood transfusions. The disease primarily involves the heart and gastrointestinal system.
  • Child abuse: Physical, sexual, emotional abuse or neglect of child.
  • Cognitive impairment: General loss of mental or cognitive ability
  • Congenital adrenal hyperplasia -- sodium-wasting form: A group of disorder that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids - a severe deficiency of 21-hydroxylase causing salt-wasting which is potentially fatal.
  • Cycad poisoning: Cycads are a green plant which has a thick trunk from the top of which sprouts palm-like leaves. Eating the seeds, leaves or unprocessed flour made from the trunk of the plant can cause various symptoms if large quantities are eaten. The harmful compounds in the plant are glycosides and BMAA
  • Cysticercosis: An infectious disease caused by the pork tapeworm Taenia solium. If the larvae are ingested then a mild or asymptomatic tapeworm infection occurs. However, ingested eggs pass into the bloodstream where they can then enter various tissues and form the cysts that characterize cysticercosis.
  • Dementia, familial British: A rare, early-onset inherited form of dementia caused by deposits of amyoid substances (amyloid) and degenerative nerve changes in the brain.
  • Depressive disorders: Depression or its various related conditions.
  • Depressive symptoms: Inappropriate depressed mood.
  • 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.
  • Dysthymia: Chronic depression usually associated with elderly people suffering stress from a variety of causes.
  • 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.
  • Emotional stress: A condition which occurs when a person is under stress affecting their emotions
  • Emotional symptoms: Symptoms affecting the emotions.
  • 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.
  • Gaucher disease -- perinatal lethal form: A rare syndrome characterized by the association of abnormally tight skin and Gaucher disease which is a lipid storage disease. This is the most severe form of Gaucher disease.
  • Granulomatous amebic encephalitis: Brain/CNS infection from Acanthamoeba bacteria
  • Granulomatous amoebic encephalitis: A rare opportunistic brain infection caused by certain amoeba - Acanthamoeba or Balamuthia amoebae. The amoeba generally only causes encephalitis in people who are immunocompromised or have a chronic disease such as diabetes. The amoeba initially cause pneumonitis or skin ulcers from with the amebas can spread to the brain to cause encephalitis. The condition is often fatal.
  • Head symptoms: Symptoms affecting the head or brain
  • Hepatic encephalopathy syndrome: A rare syndrome involving the association of advanced liver disease and neurological problems.
  • Huntington's disease: Inherited disease causing progressive mental deterioration.
  • 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.
  • Lhermitte-McAlpine syndrome: A type of neurodegenerative disorder that involves pyramidal and extrapyramidal symptoms. It can occur in middle-aged or old people and usually results in death within a year of onset.
  • Lipoid congenital adrenal hyperplasia: A rare form of congenital adrenal hyperplasia where the early phase of adrenal cortisol production is defective which causes mineralocorticoid deficiency. Male pseudohermaphroditism is the main characteristic of this disorder.
  • Loss of interest: The loss of ones interest in something
  • Loss of interest in activities: disinterest in usual daily activities
  • Marchiafava-Bignami disease: A progressive syndrome associated with alcohol abuse and/or nutritional disorder. It is characterized by fits, stupor, dementia and coma.
  • Marijuana abuse: Illicit depressant/hallucinogenic drug
  • Marijuana addiction: Marijuana addiction is the uncontrollable desire to use marijuana on a regular basis. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
  • Marijuana amotivational syndrome: Symptoms resulting from chronic marijuana use. Some experts won't recognize the symptoms as a distinctive condition.
  • Mood symptoms: Mood symptoms such as depressive symptoms and mania.
  • Movement symptoms: Changes to movement or motor abilities
  • Multiple Sclerosis: Autoimmune attack on spinal nerves causing diverse and varying neural problems.
  • Multiple Sclerosis, Susceptibility To, 1: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 1 is linked to a defect on chromosome 6p21.3.
  • Multiple Sclerosis, Susceptibility To, 2: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 2 is linked to a defect on chromosome 10p15.1.
  • Multiple Sclerosis, Susceptibility To, 3: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 3 is linked to a defect on chromosome 5p13.2.
  • Multiple Sclerosis, Susceptibility To, 4: Multiple sclerosis is a nerve or spinal cord disease that causes random damage to parts of the nervous system. The result is a diverse range of possible symptoms depending on which parts of the cord are damaged, and how often the inflammation reoccurs. Typical symptoms are any kind of tingling, numbness, burning sensations, "pins-and-needles" or other types of sensory changes in various parts of the body. Researchers have discovered that some forms of multiple sclerosis are linked to a genetic defect. Type 4 is linked to a defect on chromosome 1p36.
  • Naegleria: Rare bacterial infection from contaminated water
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurocysticercosis: Brain/CNS infection with the tapeworm Cysticercosis
  • Nielsen-Jacobs syndrome: A rare condition where damage to the part of the brain called the cingulated gyri results in agnosia, apraxia and aphasia. The cingulated gyri is responsible for emotions, memory, learning and processing skills.
  • Organic personality syndrome: Persistant personality changes due to physical causes such as a chemical imbalance rather than psychiatric causes. The duration and severity of the condition is determined by the nature and location of the cause.
  • Orotic aciduria hereditary: A rare metabolic disorder where an inherited enzyme deficiency (lack of orotidylic pyrophosphorylase and orotidylic decarboxylase or a lack of orotidylic decarboxylase only) impairs the body's ability to break down orotic acid which then builds up in the body and causes damage.
  • Oroticaciduria 1: A rare metabolic disorder where deficiency of two enzymes (orotidylic pyrophosphorylase and orotidylic decarboxylase) which impairs the body's ability to break down orotic acid which then builds up in the body where it can cause damage.
  • Orotidylic decarboxylase deficiency: A rare metabolic disorder where deficiency of an enzyme (orotidylic decarboxylase) which impairs the body's ability to break down orotic acid which then builds up in the body where it can cause damage.
  • Panic attack: A condition which is characterized by an acute episode of intense anxiety
  • Panic disorder: is a severe medical condition characterized by extremely elevated mood
  • Paralytic shellfish poisoning: Rare food poisoning from eating contaminated shellfish
  • Personality disorder: Any of a group of disorders that affect ones personality
  • Personality symptoms: Symptoms or changes to the personality.
  • Pick's Disease: Degenerative dementia condition.
  • 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.
  • Pork tapeworm: A tapeworm infection that is caused from pork
  • Post-traumatic stress disorder: Stress following a traumatic event.
  • Progressive Supranuclear Palsy: A disorder characterized by reduced motor control, dementia and eye movement problems.
  • Protein deficiency:
  • Psychiatric symptom: Psychiatric mental health symptoms such as psychosis.
  • 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.
  • Schizophrenia: A psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought.
  • Schizophrenia 1: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 1 is linked to a genetic defect on chromosome 5q23-q35.
  • Schizophrenia 10: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 10 is linked to a genetic defect on chromosome 15q15.
  • Schizophrenia 11: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 11 is linked to a genetic defect on chromosome 10q22.3.
  • Schizophrenia 12: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 12 is linked to a genetic defect on chromosome 1p36.2.
  • Schizophrenia 13: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 13 is linked to a genetic defect on chromosome 15q13.
  • Schizophrenia 14: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 14 is linked to a genetic defect on chromosome 2q32.1.
  • Schizophrenia 2: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 2 is linked to a genetic defect on chromosome 11q14-q21.
  • Schizophrenia 3: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 3 is linked to a genetic defect on chromosome 6p23.
  • Schizophrenia 4: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 4 is linked to a genetic defect on chromosome 22q11.2.
  • Schizophrenia 5: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 5 is linked to a genetic defect on chromosome 6q13-q26.
  • Schizophrenia 6: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 6 is linked to a genetic defect on chromosome 8p21 and 8p22-p11.
  • Schizophrenia 7: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 7 is linked to a genetic defect on chromosome 13q32.
  • Schizophrenia 9: Schizophrenia is a psychiatric disorder characterized by hallucinations and delusional beliefs where a person is unable to distinguish between reality and imagination. The condition tends to have a chronic nature and can be severely debilitating if treatment isn't sought. The exact cause is unknown but many experts believed that it is often the result of a genetic predisposition coupled with an environmental trigger. Type 9 is linked to a genetic defect on chromosome 1q42.1.
  • Self-esteem symptoms: Poor self image or self-esteem.
  • Spastic paraplegia 4, autosomal dominant: A rare syndrome characterized mainly by progressive stiffness and increased reflexes in the leg muscles. The severity of the condition is very variable as is the age of onset.
  • Tay Sachs Disease: A condition which is causes GM2 gangliosidosis
  • Tay-Sachs disease -- juvenile onset: A rare inherited biochemical disorder involving the deficiency of an enzyme called Hexosaminidase A. There are two forms of the disease - juvenile and adult onset.
  • Variant Creutzfeldt-Jakob disease: The bovine spongiform encephalopathy affects cattle but the variant form can infect humans. Human infection can occur by consuming infected cattle products, especially the brain and other central nervous system tissues.
  • Vitamin D -- adverse effects: Excessive use of vitamin D supplements can cause symptoms.
  • Wernicke-Korsakoff syndrome: A rare degenerative brain disorder caused by thiamine (Vitamin B1) deficiency. Chronic alcoholics are prone to this condition.
  • Whole-body acute irradiation -- hematopoietic syndrome: Tissue injury can result from exposure to radiation. The radiation dose, rate of dosing and tissues irradiated will determine the severity and type of symptoms. The effects may be chronic, delayed or acute. Hematopoietic syndrome involves exposure of the whole body to radiation of 200-1,000 rads.

Conditions listing medical symptoms: Detachment:

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Conditions listing medical complications: Detachment:

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

 

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