Iron deficiency anemia in a patient with hereditary hemorrhagic telangiectasia. Case report

Iron deficiency anemia in a patient with hereditary hemorrhagic telangiectasia. Case report

RenduOslerWeber disease or hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease. It is characterized by vascular dysplasia with the formation of telangiectasias on the skin, mucous membranes of the respiratory and digestive tracts, arteriovenous malformations (AVMs) in th...

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Bibliographic Details
Main Authors: Maria A. Mozdon, Rodion V. Ponomarev, Nina V. Tsvetaeva, Aleksey V. Shabrin, Evgeniya I. Ermachenkova, Sergei E. Larichev, Elena A. Lukina
Format: Article
Language:Russian
Published: "Consilium Medicum" Publishing house 2023-09-01
Series:Терапевтический архив
Subjects:
rendu–osler–weber disease
hereditary hemorrhagic telangiectasia
nosebleeds
iron deficiency anemia
clinical case
Online Access:https://ter-arkhiv.ru/0040-3660/article/viewFile/595930/135404

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https://ter-arkhiv.ru/0040-3660/article/viewFile/595930/135404

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