[Lysosomal storage disease].

S, Okada

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Article . 1996

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[Lysosomal storage disease].

descriptionPublicationkeyboard_double_arrow_right Article 12 Mar 1996 Japanese Journal:Nihon rinsho. Japanese journal of clinical medicine, volume 53 (issn: 0047-1852,

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Authors: S, Okada;

pmid: 8577034

[Lysosomal storage disease].

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Abstract

Lysosomes are the principal sites of intracellular digestion. In Lysosomes approximately 40 hydrolytic enzymes are contained. Lysosomal storage diseases are mainly caused by genetic defects that affect one or more of the lysosomal hydrolases, and result in accumulation of their undigested substrates in lysosomes, with profound pathological consequences. In this paper clinical features, diagnostic methods, and trend of the present research for lysosomal storage diseases are reviewed.

Related Organizations

Osaka University
Japan

Keywords

Lysosomal Storage Diseases, Humans, Mucopolysaccharidoses, Sphingolipidoses

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