A FAMILY CASE OF HEREDITARY HEMORRHAGIC TELANGIOECTASIA

Author:

Ilenkova Natalia1,Alekseeva Olga1,Chikunov Vladimir2,Pastukhova Svetlana3,Zima Andrey4

Affiliation:

1. Krasnoyarsk State Medical University named after Professor V. F. Voyno-Yasenetsky

2. Krasnoyarsk State Medical University named after Professor V. F. Voyno-Yasenetsky

3. Clinical Hospital named after I.S. Berzon

4. Krasnoyarsk Clinical Hospital named after I.S. Berzon

Abstract

The article provides an observation of the clinical detection of familial hereditary hemorrhagic telangiectasia (Osler-Weber-Rondu disease), which is manifested by a tumor of the transformation of small foci in multiple telangiectasias, on the skin, mucous and serous membranes, arteriovenous shunts in the internal organs and aneurysms, which is manifested by bleeding. This rare defect had various clinical manifestations in the mother and caused relapses of pulmonary circulation in the child and, as a result, posthemorrhagic ane mia. The given obligatory observation by a pediatrician should be directed to severe symptoms of the disease and obligatory compliance with the requirements and treatment

Publisher

Astrakhan State Medical University

Reference6 articles.

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