- * * *Term for a group of white matter diseases, some familial, characterized by progressive cerebral deterioration usually in early life, and pathologically by primary absence or degeneration of the myelin of the central and peripheral nervous systems with glial reaction; probably related to a defect in lipid metabolism; most leukodystrophies are autosomal recessive, several X-linked recessive, and a few autosomal dominant. SEE ALSO: Canavan disease. SYN: leukodystrophia cerebri progressiva, leukodystrophia, sclerosis of white matter. [leuko- + G. dys, bad, + trophe, nourishment]- adrenal l. sudanophilic l. with bronzing of skin and adrenal atrophy. A metabolic disorder of young males, characterized by widespread myelin degeneration and associated adrenal insufficiency. The myelin degeneration is massive in various portions of the brain and sometimes the spinal cord, with the accumulation of degradation products of myelin in macrophages: sudanophilic demyelination; atrophy is present in the adrenal glands and testes, and markedly increased amounts of very long-chain fatty acid are present in both the brain and adrenal glands. Symptoms include bronzing of the skin, dysarthria, cortical blindness, bilateral hemiplegia, pseudobulbar paralysis, and progressive dementia. Probably sex-linked recessive inheritance.- globoid cell l. [MIM*245200] a metabolic disorder of infancy or early childhood characterized by spasticity, seizures, and rapidly progressive cerebral degeneration, massive loss of myelin, severe astrocytic gliosis, and infiltration of the white matter with characteristic multinucleate globoid cells; metabolically there is gross deficiency of lysosomal cerebrosidase (galactosylceramide β-galactosidase); autosomal recessive inheritance, caused by mutation in the gene encoding glycosylceramidase (GALC) on 14q. SYN: diffuse infantile familial sclerosis, galactosylceramide lipoidosis, Krabbe disease.- metachromatic l. [MIM*250100] a metabolic disorder, with onset usually in the second year of life and death often before 5 years, with loss of myelin and accumulation of metachromatic lipids (galactosyl sulfatidates) in the white matter of the central and peripheral nervous systems leading to motor symptoms, paralysis, convulsions, and progressive cerebral deterioration; . Autosomal recessive inheritance [MIM*249900 and MIM*250100], caused by mutation in either the arylsulfatase A gene (ARSA) on 22q or the prosaposin gene (PSAP) on 10q. There is a dominant form occurring in adults [MIM*156310]. SYN: arylsulfatase A deficiency, sulfatide lipidosis.- l. with diffuse Rosenthal fiber formation a metabolic disorder whose onset can be in infancy, adolescence, or adulthood; characterized pathologically by widespread cerebral demyelination with astrocyte and primitive oligodendroglial cell proliferation; refractile Rosenthal fiber s result from the degeneration of these proliferating cells; etiology unknown, but possibly due to a metabolic defect of astrocytes; sex-linked recessive disorder.
* * *leu·ko·dys·tro·phy or chiefly Brit leu·co·dys·tro·phy .lü-kō-'dis-trə-fē n, pl -phies any of several inherited diseases (as adrenoleukodystrophy) characterized by progressive degeneration of myelin in the brain, spinal cord, and peripheral nerves
* * *leu·ko·dys·tro·phy (loo″ko-disґtrə-fe) any of various types of neurodegeneration involving disturbance of the white matter of the brain. See also adrenoleukodystrophy and leukoencephalopathy.
Medical dictionary. 2011.
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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 — noun (plural phies) Date: 1960 any of several genetically determined diseases characterized by progressive degeneration of myelin in the brain, spinal cord, and peripheral nerves … New Collegiate Dictionary
leukodystrophy — noun Any of a group of disorders characterized by progressive degeneration of the white matter of the brain, caused by imperfect growth or development of the myelin sheath that acts as an insulator around nerve fibres … Wiktionary
leukodystrophy — leu·ko·dys·tro·phy … English syllables
leukodystrophy — ˌlükōˈdistrəfē noun Etymology: leuc + dystrophy : any of several genetically determined diseases (as adrenoleukodystrophy) characterized by progressive degeneration of myelin in the brain, spinal cord, and peripheral nerves … Useful english dictionary
Metachromatic leukodystrophy — Classification and external resources Sulfatide ICD 10 E75.2 … Wikipedia
globioid cell leukodystrophy — globioid cell leukodystrophy. = Krabbe disease (см.). (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
globioid cell leukodystrophy — globioid cell leukodystrophy. См. болезнь Краббе. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
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
Krabbe disease (leukodystrophy) — Krab·be disease (leukodystrophy) (krahґbə) [Knud H. Krabbe, Danish neurologist, 1885â€“1961] see under disease … Medical dictionary