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- W2024483815 abstract "Miyoshi myopathy is the most common form of recessive distal myopathy. Recessive mutations in the ANO5 gene have been recently identified in Northern Europe as a cause of non dysferlin-linked distal myopathy and limb girdle muscular dystrophy. We report here the first French cases of anoctamin 5 myopathy in 2 brothers presenting with a Miyoshi-like pattern. Comparing these patients with 12 other cases from the literature shows that all cases share a homogeneous clinical pattern, characterized by initial calf muscles involvement. Asymmetric muscle atrophy often precedes weakness. In this setting, high CK level and normal expression of dysferlin in muscle should lead to consider the diagnosis, which will be confirmed by ANO5 gene testing. The c.191dupA mutation, already reported as a founder mutation in Caucasian patients with anoctamin myopathies, was found in our family in a heterozygous state." @default.
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- W2024483815 date "2012-02-01" @default.
- W2024483815 modified "2023-09-30" @default.
- W2024483815 title "Miyoshi-like distal myopathy with mutations in anoctamin 5 gene" @default.
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- W2024483815 doi "https://doi.org/10.1016/j.neurol.2011.10.005" @default.
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