The hereditary progressive muscular dystrophy type 2A (calpainopathy): a clinical case
https://doi.org/10.17650/2222-8721-2015-1-42-47
Abstract
Presents clinical case the hereditary progressive muscular dystrophy type 2A (calpainopathy). Shows diagnostic difficulties and feature of presents clinical observations. This case is significance, as in the domestic scientific literature presents few articles on clinical examples of this muscle pathology.
About the Authors
D. A. Grishina
Research Center of Neurology, Russian Academy of Medical Sciences
Russian Federation
Research and Consulting Department, 80, Volokolamskoe Shosse, Moscow 125367, Russia
Russian Federation
Research and Consulting Department, 80, Volokolamskoe Shosse, Moscow 125367, Russia
N. A. Suponeva
Research Center of Neurology, Russian Academy of Medical Sciences
Russian Federation
Department of Neurorehabilitation and Physiotherapy, 80, Volokolamskoe Shosse, Moscow 125367, Russia
Russian Federation
Department of Neurorehabilitation and Physiotherapy, 80, Volokolamskoe Shosse, Moscow 125367, Russia
V. V. Shvedkov
Research Center of Neurology, Russian Academy of Medical Sciences
Russian Federation
Research and Consulting Department, 80, Volokolamskoe Shosse, Moscow 125367, Russia
Russian Federation
Research and Consulting Department, 80, Volokolamskoe Shosse, Moscow 125367, Russia
A. V. Belopasova
Research Center of Neurology, Russian Academy of Medical Sciences
Russian Federation
Neurology Department Three, 80, Volokolamskoe Shosse, Moscow 125367, Russia
Russian Federation
Neurology Department Three, 80, Volokolamskoe Shosse, Moscow 125367, Russia
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Review
For citations:
Grishina D.A., Suponeva N.A., Shvedkov V.V., Belopasova A.V. The hereditary progressive muscular dystrophy type 2A (calpainopathy): a clinical case. Neuromuscular Diseases. 2015;5(1):42-47. (In Russ.) https://doi.org/10.17650/2222-8721-2015-1-42-47
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