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PMID: 4470886 Published · ppublish English Journal Article

Cystinosis.

Birth defects original article series ·Vol. 10 ·No. 4 ·1974-00-00 ·Pages 114-7

Schulman JD

Abstract

This paper about cystinosis is focused primarily on nosology and genetic heterogeneity, the recurrent themes of these conferences. It briefly discusses cystinosis in relation to other disorders which cause the renal Fanconi syndrome with or without glomerular insufficiency, points out the methods for its reliable diagnosis, and then summarizes evidence suggesting that cystinosis should be classified as one of the lysosomal storage diseases. More extensive reviews of cystinosis are available.

MeSH Terms
Child Conjunctiva/metabolism Cystine/metabolism Cystinosis/genetics,pathology Fanconi Syndrome/etiology Genotype Humans Kidney/metabolism Lysosomes/metabolism Phenotype
Chemicals
Cystine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Schulman J D
Article Info
Journal
Birth defects original article series
Abbr.
Birth Defects Orig Artic Ser
ISSN
0547-6844
Published
1974-00-00
Pages
114-7
Language
English
Region
United States
NLM ID
0003403
Subset
IM
External Links
PubMed source
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