These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Setleis syndrome: autosomal recessive or autosomal dominant inheritance?
    Author: al-Gazali LI, al-Talabani J.
    Journal: Clin Dysmorphol; 1996 Jul; 5(3):249-53. PubMed ID: 8818454.
    Abstract:
    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.
    [Abstract] [Full Text] [Related] [New Search]