muramidase and Mucopolysaccharidoses

muramidase has been researched along with Mucopolysaccharidoses* in 2 studies

Other Studies

2 other study(ies) available for muramidase and Mucopolysaccharidoses

Article	Year
Juvenile neurogenic muscle atrophy with lysosomal enzyme deficiencies: new disease or variant of mucopolysaccharidosis? Journal of neurology, 1983, Volume: 229, Issue:1 An 18-year-old boy showed childhood onset of mental retardation, neurogenic muscle atrophy with hyperreflexia, Marfan-like features, multiple epiphyseal dysplasia, increased urinary excretion of dermatan sulfate, and decreased lysosomal enzyme activities in beta-galactosidase, beta-glucuronidase, and N-acetyl-beta-D-glucosaminidase. This case may be a new syndrome, the combination of neurogenic muscle atrophy with lysosomal enzyme deficiencies. Topics: Adolescent; Diagnosis, Differential; Humans; Intellectual Disability; Leukocytes; Male; Metabolism, Inborn Errors; Mucopolysaccharidoses; Muramidase; Muscular Atrophy; Reflex, Abnormal; Syndrome	1983
[Biochemical bases of the hematological aspects of the diseases caused by the accumulation of glycolipids, mucopolysaccharides and oligosaccharides]. Minerva medica, 1975, Jul-11, Volume: 66, Issue:50 Topics: Erythrocytes; Glycolipids; Glycosaminoglycans; Glycosphingolipids; Granulocytes; Humans; Lipid Metabolism; Lipidoses; Lymphocytes; Macrophages; Metabolic Diseases; Mucopolysaccharidoses; Muramidase; Oligosaccharides; Phagocytosis; Phospholipids	1975

Article

Year

Juvenile neurogenic muscle atrophy with lysosomal enzyme deficiencies: new disease or variant of mucopolysaccharidosis?

Journal of neurology, 1983, Volume: 229, Issue:1

An 18-year-old boy showed childhood onset of mental retardation, neurogenic muscle atrophy with hyperreflexia, Marfan-like features, multiple epiphyseal dysplasia, increased urinary excretion of dermatan sulfate, and decreased lysosomal enzyme activities in beta-galactosidase, beta-glucuronidase, and N-acetyl-beta-D-glucosaminidase. This case may be a new syndrome, the combination of neurogenic muscle atrophy with lysosomal enzyme deficiencies.

Topics: Adolescent; Diagnosis, Differential; Humans; Intellectual Disability; Leukocytes; Male; Metabolism, Inborn Errors; Mucopolysaccharidoses; Muramidase; Muscular Atrophy; Reflex, Abnormal; Syndrome

1983

[Biochemical bases of the hematological aspects of the diseases caused by the accumulation of glycolipids, mucopolysaccharides and oligosaccharides].

Minerva medica, 1975, Jul-11, Volume: 66, Issue:50

Topics: Erythrocytes; Glycolipids; Glycosaminoglycans; Glycosphingolipids; Granulocytes; Humans; Lipid Metabolism; Lipidoses; Lymphocytes; Macrophages; Metabolic Diseases; Mucopolysaccharidoses; Muramidase; Oligosaccharides; Phagocytosis; Phospholipids

1975