Family form of dilated cardiomyopathy
D. I. Sadykova, 
T. P. Makarova,
D. R. Sabirova,
N. N. Firsova,
A. A. Kucheryavaya,
N. V. Shakurova,
A. R. Khasanova
T. P. Makarova,
D. R. Sabirova,
N. N. Firsova,
A. A. Kucheryavaya,
N. V. Shakurova,
A. R. Khasanova https://doi.org/10.21508/1027-4065-2021-66-5-202-206
Abstract
Cardiomyopathy (CMP) is classified into familial and non-familial, which reflects the need to study the genetic basis of the disease. The article describes a clinical case of a familial form of non-compact cardiomyopathy in combination with a dilated form of cardiomyopathy. The article provides data of echocardiographic and MRI studies. The diagnosis was confirmed by genetic research, there was revealed a mutation in the MYH7 gene p.IIe201Thr in a heterozygous state, which is associated with the development of non-compact cardiomyopathy and dilated form of cardiomyopathy.
About the Authors
D. I. Sadykova
Kazan State Medical University
Russian Federation
Russian Federation
Kazan
T. P. Makarova
Kazan State Medical University
Russian Federation
Russian Federation
Kazan
D. R. Sabirova
Kazan State Medical University
Russian Federation
Russian Federation
Kazan
N. N. Firsova
Children’s Republican Clinical Hospital
Russian Federation
Russian Federation
Kazan
A. A. Kucheryavaya
Children’s Republican Clinical Hospital
Russian Federation
Russian Federation
Kazan
N. V. Shakurova
Kazan State Medical University
Russian Federation
Russian Federation
Kazan
A. R. Khasanova
Kazan State Medical University
Russian Federation
Russian Federation
Kazan
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Review
For citations:
Sadykova D.I., Makarova T.P., Sabirova D.R., Firsova N.N., Kucheryavaya A.A., Shakurova N.V., Khasanova A.R. Family form of dilated cardiomyopathy. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2021;66(5):202-206. (In Russ.) https://doi.org/10.21508/1027-4065-2021-66-5-202-206
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