Document Detail


Pseudohypoparathyroidism associated with cri du chat syndrome.
MedLine Citation:
PMID:  995018     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A case is reported in which features of pseudohypoparathyroidism were found in association with the cri du chat syndrome. This association may throw some light on the localization of the chromosomal abberration which underlies pseudohypoparathyroidism, since deletion of the short arm of chromosome 5 has been clearly established in the cri du chat syndrome.
Authors:
C W Kee; P Lim; I K Tan
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Medical journal of Australia     Volume:  2     ISSN:  0025-729X     ISO Abbreviation:  Med. J. Aust.     Publication Date:  1976 Aug 
Date Detail:
Created Date:  1977-01-25     Completed Date:  1977-01-25     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0400714     Medline TA:  Med J Aust     Country:  AUSTRALIA    
Other Details:
Languages:  eng     Pagination:  344-5     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Child
Chromosome Deletion
Chromosomes, Human, 4-5
Cri-du-Chat Syndrome / complications*,  genetics
Female
Humans
Male
Pseudohypoparathyroidism / complications*,  genetics

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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