Alexander disease is a rare disorder of the nervous system. It is considered one of the leukodystrophies, a group of disorders in which the primary abnormality is the inability to maintain myelin.
Alexander disease Overview Alexander disease (ALX) is a rare and often fatal nervous system disorder that primarily occurs in infants and children.
Alexander Disease National Organization for Rare Disorders, Inc. Synonyms ...
Alexander Disease By Dawn J. Cardeiro MS, CGCThe Gale Group Inc., Gale.. Gale Encyclopedia of Neurological Disorders, 2005more » Definition ...
NINDS Alexander Disease Information Page Skip secondary menu Home Disorders A - Z ...
What is Alexander disease? Alexander disease is a rare disorder of the nervous system. It is one of a group of disorders, called leukodystrophies, that involve the destruction of myelin.
Alexander disease, ORI, HPB, CC, NIOSH, NEFLE, Dental Ethic, Dental Root Cyst, Dihydroxyacetone Phosphate, Ependymoma, Clear Cell, Epidemiologic Determinants, Folk Remedy, Geriatrics, Glycerophosphate, Choline, Hemoglobinuria, Interaction Map, ...
Alexander Disease Alexander Graham Bell Association for Deaf and Hard of Hearing - Support Group Alexander Graham Bell Association for Deaf and Hard of Hearing - Deaf / Hearing Impaired / Tinnitus / Meniere's - Support Group ...
Alexander disease Alexander Leukodystrophy see Alexander disease Alkaptonuria ALL see Leukaemia and other Allied Blood disorders Allergies Alobar HPE see Holoprosencephaly Alopecia Alopecia Areata see Alopecia Alopecia Totalis see Alopecia ...
Of the 3 subtypes of Alexander disease (infantile, juvenile, and adult), all three have been proven to be caused by mutations in GFAP. More than 20 GFAP mutations that cause Alexander disease have been identified.
Overuse of medicines may be the single biggest cause of nervous system problems in older adults. Alexander Disease Causes, Symptoms And Treatment And Related Disorders ...
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GFAP (Glial Fibrillary Acidic Protein): The degenerative brain condition called Alexander disease is caused by mutation in GFAP (glial fibrillary acidic protein).
Pelizaeus-Merzbacher disease Canavan disease Childhood ataxia with central nervous system hypomyelination (CACH, also called vanishing white matter disease) Alexander disease Refsum disease Cerebrotendinous xanthomatosis ...
metachromatic leukodystrophy, Krabbé disease, adrenoleukodystrophy, Pelizaeus-Merzbacher disease, Canavan disease, Childhood Ataxia with Central Nervous System Hypomyelination or CACH (also known as Vanishing White Matter Disease), Alexander disease, ...
See also: Dystrophy, Symptom, Leukodystrophy, Ataxia, Central nervous system
 
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