THE CASE OF ERB-ROTH’S NEUROMUSCULAR DISTROPHY
https://doi.org/10.17802/2306-1278-2018-7-1-102-104
Abstract
The article presents a clinical case of a patient with Erb-Roth’s hereditary neuromuscular dystrophy presented with severe cardiomyopathy.
About the Authors
A. N. LobanovaRussian Federation
Corresponding author: Lobanova Anna, address: Russian Federation, 660022, Krasnoyarsk, Partizana Zheleznyaka Street, 1
M. M. Petrova
Russian Federation
Krasnoyarsk
E. I. Harkov
Russian Federation
Krasnoyarsk
N. U. Tsibulskaya
Russian Federation
Krasnoyarsk
References
1. Sharkova I.V., Dadali E.L., Ugarov I.V., Ryzhkova O.P., Poljakov A.V. Sravnitel’nyj analiz osobennostej fenotipov dvuh rasprostranennyh geneticheskih variantov pojasnokonechnostnoj myshechnoj distrofii. Nervno-myshechnye bolezni 2015; 5: 42-48. (In Russ).
2. Angelini C., Nardetto L., Fanin M., Nascimbeni A-C., Tasca E. Heterogeneous pathogenesis of LGMD2: consequences for therapy. Basic applied mycology. 2007; 17: 173-179.
3. Dadali E.L., Shagina O.A., Ryzhkova O.P., Rudenskaja G.E., Fedotov V.P., Poljakov A.V. Klinikogeneticheskie harakteristiki pojasno-konechnostnoj myshechnoj distrofii 2A tipa. Zhurnal nevrologii i psihiatrii im. S.S. Korsakova. 2010; 4: 79-83. (In Russ).
4. Strahova O.S., Belozerov Ju.M. Osobennosti lechenija kardiomiopatij u bol’nyh s progressirujushhej myshechnoj distrofiej. Pediatricheskaja farmakologija, 2003; 2: 61-64. (In Russ).
Review
For citations:
Lobanova A.N., Petrova M.M., Harkov E.I., Tsibulskaya N.U. THE CASE OF ERB-ROTH’S NEUROMUSCULAR DISTROPHY. Complex Issues of Cardiovascular Diseases. 2018;7(1):102-104. (In Russ.) https://doi.org/10.17802/2306-1278-2018-7-1-102-104