Document Detail


Hereditary sclerosing poikiloderma.
MedLine Citation:
PMID:  659034     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Three persons with hereditary sclerosing poikiloderma were studied to find any clue to explain the mechanism involved in producing the cutaneous lesions which are so striking clinically and also evident histologically. Investigational studies included a blood chemistry screen, chromosome analyses, and skin biopsies evaluated by routine stains as well as by electron microscopy and direct immunofluorescence. No mechanism for the production of the clinical and histological changes in the dominantly inherited disorder was found.
Authors:
K E Greer; P E Weary; R Nagy; M Robinow
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  International journal of dermatology     Volume:  17     ISSN:  0011-9059     ISO Abbreviation:  Int. J. Dermatol.     Publication Date:  1978 May 
Date Detail:
Created Date:  1978-08-14     Completed Date:  1978-08-14     Revised Date:  2006-10-30    
Medline Journal Info:
Nlm Unique ID:  0243704     Medline TA:  Int J Dermatol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  316-22     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Child
Diagnosis, Differential
Humans
Male
Rothmund-Thomson Syndrome / diagnosis,  genetics*,  pathology
Skin / pathology
Skin Diseases / genetics*

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