- metachromatic leukodystrophy
- Медицина: метахроматическая лейкодистрофия
Универсальный англо-русский словарь. Академик.ру. 2011.
metachromatic leukodystrophy
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Metachromatic leukodystrophy — Classification and external resources Sulfatide ICD 10 E75.2 … Wikipedia
metachromatic leukodystrophy — n a hereditary neurological disorder of lipid metabolism characterized by the accumulation of cerebroside sulfates, loss of myelin in the central nervous system, and progressive deterioration of mental and motor activity * * * an autosomal… … Medical dictionary
metachromatic leukodystrophy — ▪ pathology rare inherited metabolic disease in which the lack of a key enzyme causes loss of the protective myelin sheath from the white matter of the brain, resulting in psychological disturbances, mental deterioration, and sensory and… … Universalium
Leukodystrophy — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 32504 ICD10 = ICD10|E|71|3|e|70, ICD10|E|75|2|e|70 ICD9 = ICD9|330.0 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Leukodystrophy refers to a group of disorders… … Wikipedia
Leukodystrophy — A disorder of the white matter of the brain, the part of the brain that contains myelinated nerve fibers. The white matter is white because it is the color of myelin, the insulation covering the nerve fibers. (The white matter is as opposed to… … Medical dictionary
metachromatic leukoencephalopathy — see under leukodystrophy … Medical dictionary
sulfatide lipidosis — metachromatic leukodystrophy … Medical dictionary
Arylsulfatase A — PDB rendering based on 1auk … Wikipedia
Prosaposin — PDB rendering based on 1m12 … Wikipedia
Psychosis — Not to be confused with Psychopathy. For other uses, see Psychosis (disambiguation). Psychosis Classification and external resources ICD 10 F20 F29[1] ICD 9 … Wikipedia
Leukoencephalopathy with vanishing white matter — Classification and external resources OMIM 603896 Leukoencephalopathy with vanishing white matter (VWM disease) is an autosomal recessive neurological disease. The cause of the disease are mutations in any of the 5 genes encoding subunits of the… … Wikipedia
