Combination of tetralogy of Fallot and hemophilia in a child: case report

dc.contributor.author	Piddubna, I.
dc.contributor.author	Kulikova, D.
dc.contributor.author	Pisclova, Y.
dc.contributor.author	Buchnieva, O.
dc.date.accessioned	2019-11-15T19:26:33Z
dc.date.available	2019-11-15T19:26:33Z
dc.date.issued	2019
dc.description.abstract	Congenital heart disease (CHD) is formed during intrauterine period but, as a rule, they are not hereditary. Hemophilia A belongs to the group of hereditary coagulopathies stipulated by deficiency of coagulation factor VIII and characterized by bleeding of hematoma like type. Combination of these two diseases is rather rare that requires cardiosurgeons’ apprehensive attitude. We present our experience in surgical treatment of a boy of 8 months old with Tetralogy of Fallot. Hemophilia A was found in preoperative examination.	ru_RU
dc.identifier.citation	Combination of tetralogy of Fallot and hemophilia in a child: case report / I. N. Piddubna, D. O. Kulikova, Y. V. Pisclova, O. V. Buchnieva // World Science. ‒ 2019. ‒ N 7 (47), Vol. 1. ‒ P. 125‒127.	ru_RU
dc.identifier.uri	https://repo.knmu.edu.ua/handle/123456789/24628
dc.language.iso	en	ru_RU
dc.subject	tetralogy Fallot	ru_RU
dc.subject	hemophilia	ru_RU
dc.title	Combination of tetralogy of Fallot and hemophilia in a child: case report	ru_RU
dc.type	Article	ru_RU

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