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Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?

โœ Scribed by C. Pizzanelli; M. Mancuso; R. Galli; A. Choub; M. Fanin; A. C. Nascimbeni; G. Siciliano; L. Murri

Publisher
Springer Milan
Year
2006
Tongue
English
Weight
67 KB
Volume
27
Category
Article
ISSN
1590-1874

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We report on the clinical, pathological, and genetic features of 7 patients with limb-girdle muscular dystrophy type 2A (LGMD2A) from three Japanese families. The mean age of onset was 9.7 ยฑ 3.1 years (mean ยฑ SD), and loss of ambulance occurred at 38.5 ยฑ 2.1 years. Muscle atrophy was predominant in