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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Prif Awduron:	Maria A. Mozdon, Rodion V. Ponomarev, Nina V. Tsvetaeva, Aleksey V. Shabrin, Evgeniya I. Ermachenkova, Sergei E. Larichev, Elena A. Lukina
Fformat:	Artigo
Iaith:	Russo
Cyhoeddwyd:	"Consilium Medicum" Publishing house 2023-09-01
Cyfres:	Терапевтический архив
Pynciau:	rendu–osler–weber disease hereditary hemorrhagic telangiectasia nosebleeds iron deficiency anemia clinical case
Mynediad Ar-lein:	https://ter-arkhiv.ru/0040-3660/article/viewFile/595930/135404
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