Asian Journal of Case Reports in Medicine and Health

Rendu-Osler-Weber Syndrome: A Rare Case Report and Literature Review

Salma Ouahid *

Gastroenterology I Unit, Mohamed V Military Teaching Hospital, Rabat, Morocco.

Tarik Adioui

Gastroenterology I Unit, Mohamed V Military Teaching Hospital, Rabat, Morocco.

Chaimaa Jioua

Gastroenterology I Unit, Mohamed V Military Teaching Hospital, Rabat, Morocco.

Imane Radouane

Gastroenterology I Unit, Mohamed V Military Teaching Hospital, Rabat, Morocco.

Jihane Benass

Gastroenterology I Unit, Mohamed V Military Teaching Hospital, Rabat, Morocco.

Sanaa Berrag

Gastroenterology I Unit, Mohamed V Military Teaching Hospital, Rabat, Morocco.

Mouna Tamzaourte

Gastroenterology I Unit, Mohamed V Military Teaching Hospital, Rabat, Morocco.

*Author to whom correspondence should be addressed.

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Abstract

Rendu-Osler disease is a rare inherited vascular disorder. Through this article, the authors recall the digestive manifestations of this condition, which when associated with other clinical signs, are sufficiently characteristic to allow the gastroenterologist to suggest the diagnosis.

Keywords: Telangiectasia, Rendu-Osler-Weber disease, iron deficiency anemia

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