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
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