Document Detail


The Sturge-Weber syndrome.
MedLine Citation:
PMID:  7056930     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The Sturge-Weber syndrome is a congenital anomaly that is characterized principally by unilateral angiomatosis of the skin, cerebral meninges and choroid of the eye. It may be attended by mental retardation, convulsions, hemiplegia, and visual disturbances. The complete syndrome is rare. We herewith report a case of the syndrome fairly fully developed.
Authors:
C E Kouskoukis; C J Kanitakis
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Journal of dermatologic surgery and oncology     Volume:  8     ISSN:  0148-0812     ISO Abbreviation:  J Dermatol Surg Oncol     Publication Date:  1982 Jan 
Date Detail:
Created Date:  1982-04-22     Completed Date:  1982-04-22     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7707501     Medline TA:  J Dermatol Surg Oncol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  47-50     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adult
Angiomatosis / diagnosis*
Humans
Male
Sturge-Weber Syndrome / diagnosis*

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


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