DILATED CARDIOMYOPATHY AGAINST THE BACKGROUND OF CENTRONUCLEAR MYOPATHY TYPE 5 IN AN 8-YEAR-OLD CHILD: A CLINICAL CASE

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DC Field	Value	Language
dc.contributor.author	Anikeeva N.A., Belykh N.A., Lashko A.Yu., Karimov Yu.D., Smetanina E.A., Fokicheva N.N., Faletrov M.V., Avezova G.S., Sultanova N.S., Mallayev Sh.Sh.	-
dc.date.accessioned	2024-12-11T09:19:52Z	-
dc.date.available	2024-12-11T09:19:52Z	-
dc.date.issued	2024	-
dc.identifier.uri	http://repo.tma.uz/xmlui/handle/1/284	-
dc.description.abstract	Dilated cardiomyopathy (DCM) represents a rare diagnosis in pediatric practice. We described the case of DCM, developed against the background of centronuclear myopathy type 5 (CNM5) in a girl 8 years old. Manifestation of the disease with neurological symptoms and presence of previously undescribed SPEG mutation has hampered and delayed timely diagnosis and treatment of the disease. Attempts of conservative and operative correction of the decompensated heart failure (HF) in this case were unsuccessful.	en_US
dc.language.iso	en_US	en_US
dc.publisher	Ўзбекистон, Тошкент	en_US
dc.relation.ispartofseries	UDK;61.616	-
dc.subject	dilated cardiomyopathy, centronuclear myopathy type 5, treatment.	en_US
dc.title	DILATED CARDIOMYOPATHY AGAINST THE BACKGROUND OF CENTRONUCLEAR MYOPATHY TYPE 5 IN AN 8-YEAR-OLD CHILD: A CLINICAL CASE	en_US
dc.type	Article	en_US
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