arylsulfatase A deficiency

arylsulfatase A deficiency
ar·yl·sul·fa·tase A de·fi·cien·cy (ar″əl-sulґfə-tās) metachromatic leukodystrophy.

Medical dictionary. 2011.

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  • 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

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