Document Detail


Setleis syndrome: autosomal recessive or autosomal dominant inheritance?
MedLine Citation:
PMID:  8818454     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Setleis syndrome is a rare skin disorder characterized by congenital scar-like depressions on the temples and distinctive facial appearance. We report on two cases from a consanguineous Omani family, with typical features of this syndrome. The mother in one case has mild dysmorphic features reminiscent of this syndrome and the father of the other case has bitemporal scars only.
Authors:
L I al-Gazali; J al-Talabani
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Clinical dysmorphology     Volume:  5     ISSN:  0962-8827     ISO Abbreviation:  Clin. Dysmorphol.     Publication Date:  1996 Jul 
Date Detail:
Created Date:  1996-12-16     Completed Date:  1996-12-16     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  9207893     Medline TA:  Clin Dysmorphol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  249-53     Citation Subset:  IM    
Affiliation:
Department of Paediatrics, Faculty of Medicine and Health Sciences, UAE University, Al Ain, UAE.
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MeSH Terms
Descriptor/Qualifier:
Adult
Consanguinity
Face / abnormalities*
Female
Genes, Dominant*
Genes, Recessive*
Humans
Infant, Newborn
Male
Pedigree
Skin Diseases / genetics*
Syndrome

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


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