The hereditary progressive muscular dystrophy type 2A (calpainopathy): a clinical case

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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.

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D. A. Grishina

Research Center of Neurology, Russian Academy of Medical Sciences

Author for correspondence.
Email: DGrishina82@gmail.com
Research and Consulting Department, 80, Volokolamskoe Shosse, Moscow 125367, Russia Russian Federation

N. A. Suponeva

Research Center of Neurology, Russian Academy of Medical Sciences

Department of Neurorehabilitation and Physiotherapy, 80, Volokolamskoe Shosse, Moscow 125367, Russia Russian Federation

V. V. Shvedkov

Research Center of Neurology, Russian Academy of Medical Sciences

Research and Consulting Department, 80, Volokolamskoe Shosse, Moscow 125367, Russia Russian Federation

A. V. Belopasova

Research Center of Neurology, Russian Academy of Medical Sciences

Neurology Department Three, 80, Volokolamskoe Shosse, Moscow 125367, Russia Russian Federation

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Copyright (c) 2015 Grishina D.A., Suponeva N.A., Shvedkov V.V., Belopasova A.V.

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