Generalized gangliosidosis: Acid β-galactosidase deficiency with early onset, rapid mental deterioration and minimal bone dysplasia View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1976-12

AUTHORS

H. Fricker, J. S. O'Brien, F. Vassella, E. Gugler, J. P. Mühlethaler, M. Spycher, U. N. Wiesmann, N. Herschkowitz

ABSTRACT

This report concerns a 3-month-old girl with rapidly progressive psychomotor retardation, hepatomegaly, vacuolated lymphocytes, minimal bone dysplasia and normal excretion of acid mucopolysaccharides. A deficiency of acid beta-galactosidase was demonstrated in isolated leucocytes and in a liver biopsy. The diagnosis of generalized gangliosidosis due to deficiency of beta-galactosidase was also based on the absence of the enzyme activity from cultured fibroblasts. The diagnosis was confirmed on autopsy at 16 months by typical histology, electron microscopy and biochemistry of the organs. beta-galactosidase deficiency has been demonstrated in various clinical conditions ranging from generalized gangliosidosis with severe mental retardation to clinical pictures resembling Morquio's disease and normal intelligence. The heterogeneity of the clinical manifestations in beta-galactosidase deficiency could be explained by different residual activities of a structurally mutated enzyme towards its various substrates. More... »

PAGES

273-281

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00316267

DOI

http://dx.doi.org/10.1007/bf00316267

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1047153579

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/62026


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