THE CLINICAL CASE OF STARK–KAESER TYPE SCAPULOPERONEAL SYNDROME

We present a rare case of Stark–Kaeser type scapuloperoneal syndrome type with mild weakness and hypotrophy in proximal limb, with rough paresis of feet, walking dysfunction and slowly-progressive course. The article briefly describes current views on the etiology and pathogenesis of this disease. T...

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Bibliographic Details
Main Authors: T. A. Valikova, V. M. Alifirova, I. V. Bychkova, K. Yu. Sabashkina
Format: Article
Language:English
Published: Siberian State Medical University (Tomsk) 2015-12-01
Series:Бюллетень сибирской медицины
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Online Access:https://bulletin.ssmu.ru/jour/article/view/387
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Summary:We present a rare case of Stark–Kaeser type scapuloperoneal syndrome type with mild weakness and hypotrophy in proximal limb, with rough paresis of feet, walking dysfunction and slowly-progressive course. The article briefly describes current views on the etiology and pathogenesis of this disease. The case is of interest to physicians of various specialties for the differential diagnosis of inherited neuromuscular disorders.
ISSN:1682-0363
1819-3684