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

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