Document Detail

Setleis syndrome: autosomal recessive or autosomal dominant inheritance?
MedLine Citation:
PMID:  8818454     Owner:  NLM     Status:  MEDLINE    
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.
L I al-Gazali; J al-Talabani
Related Documents :
18501694 - Catel-manzke syndrome: two new patients and a critical review of the literature.
3303344 - Familial intrahepatic cholestatic syndromes.
20497874 - Pulmonary manifestations and management of proteus syndrome.
3706414 - Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.
20369774 - Lupus anticoagulant, antiphospholipid syndrome and cardiac surgery.
23241824 - Corneal erosion and kindler syndrome.
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    
Department of Paediatrics, Faculty of Medicine and Health Sciences, UAE University, Al Ain, UAE.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Face / abnormalities*
Genes, Dominant*
Genes, Recessive*
Infant, Newborn
Skin Diseases / genetics*

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

Previous Document:  Three infants of diabetic mothers with malformations of left-right asymmetry--further evidence for t...
Next Document:  Reverse perfusion pattern of Tc-99m MIBI heralding the development of myocardial infarction.