- arylsulfatase A deficiency
- ar·yl·sul·fa·tase A de·fi·cien·cy (ar″əl-sulґfə-tās) metachromatic leukodystrophy.
Medical dictionary. 2011.
Medical dictionary. 2011.
arylsulfatase B deficiency — ar·yl·sul·fa·tase B de·fi·cien·cy (ar″əl sulґfə tās) Maroteaux Lamy syndrome … Medical dictionary
Arylsulfatase A — PDB rendering based on 1auk … Wikipedia
Arylsulfatase B — Crystallographic structure of putative tetrameric arylsulfatase from Escherichia coli.[1] Identifiers … Wikipedia
Arylsulfatase B — Bändermodell der Arylsulfatase B, nach PDB … Deutsch Wikipedia
Arylsulfatase A — Monomer der (489 aa) Einheit der Arylsulfatase A, nach PDB … Deutsch Wikipedia
deficiency — An insufficient quantity of some substance (as in dietary d. or hemoglobin d. in marrow aplasia); organization (as in mental d.); activity (as in enzyme d. or reduced oxygen carrying capacity of the blood), etc., of which the amount present is of … Medical dictionary
Metachromatic leukodystrophy — Classification and external resources Sulfatide ICD 10 E75.2 … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … 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
Leucodystrophie Métachromatique — Autre nom Déficit en arylsulfatase A Référence MIM … Wikipédia en Français