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Metachromatic leukodystrophy. Ultrastructural and enzymatic study of a case of variant O form

Archives of Neurology

Dec 1, 1975

E J RaynaudR Lagarde

PMID: 985

Abstract

A variant of metachromatic leukodystrophy (MLD), Austin disease, is characterized by a multiple isozyme deficiency of arylsulfatase. A 3 1/2-year-old girl with progressive mental and physical deterioration had decreased activities of arylsulfatases A and B in the leukocytes, shown by ac...read more

Mentioned in this Paper

Leukodystrophy, Metachromatic
Mucopolysaccharidosis III
Mucopolysaccharidosis VI
Arylsulfatase A Deficiency
Metabolic Syndrome X
Leukocytes
Perineurium
Structure of Broca's Area
Cerebroside-Sulfatase
Chondro-4-Sulfatase
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Metachromatic leukodystrophy. Ultrastructural and enzymatic study of a case of variant O form

Archives of Neurology

Dec 1, 1975

E J RaynaudR Lagarde

PMID: 985

DOI:

Abstract

A variant of metachromatic leukodystrophy (MLD), Austin disease, is characterized by a multiple isozyme deficiency of arylsulfatase. A 3 1/2-year-old girl with progressive mental and physical deterioration had decreased activities of arylsulfatases A and B in the leukocytes, shown by ac...read more

Mentioned in this Paper

Leukodystrophy, Metachromatic
Mucopolysaccharidosis III
Mucopolysaccharidosis VI
Arylsulfatase A Deficiency
Metabolic Syndrome X
Leukocytes
Perineurium
Structure of Broca's Area
Cerebroside-Sulfatase
Chondro-4-Sulfatase

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