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Indian Journal of Dermatology, Venereology and Leprology
Medknow Publications on behalf of The Indian Association of Dermatologists, Venereologists and Leprologists (IADVL)
ISSN: 0378-6323
EISSN: 0378-6323
Vol. 75, No. 1, 2009, pp. 100-100
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Bioline Code: dv09032
Full paper language: English
Document type: Case Report
Document available free of charge
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Indian Journal of Dermatology, Venereology and Leprology, Vol. 75, No. 1, 2009, pp. 100-100
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Osler-Weber-Rendu Syndrome: A Case Report With Familial Clustering
Grover, Sanjiv; Grewal, R.S.; Verma, Rajesh; Sahni, H.; Muralidhar, R. & Sinha, Preema
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.
Keywords
Familial, Hereditary, Telangiectasia
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© Copyright 2009 Indian Journal of Dermatology, Venereology and Leprology.
Alternative site location: http://www.ijdvl.com
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