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

Search MEDLINE/PubMed


  • Title: Osler-Weber-Rendu syndrome: a case report with familial clustering.
    Author: Grover S, Grewal RS, Verma R, Sahni H, Muralidhar R, Sinha P.
    Journal: Indian J Dermatol Venereol Leprol; 2009; 75(1):100-1. PubMed ID: 19180693.
    Abstract:
    Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder manifested by telangiectases of the skin and mucous membranes and arteriovenous malformations of various organ systems. We present a case of Osler-Weber-Rendu syndrome with 11 affected members in her family.
    [Abstract] [Full Text] [Related] [New Search]