| Literature DB >> 17614318 |
Hiroshi Saito1, Naoki Suzuki, Hideaki Ishiguro, Koichi Hirota, Yasuto Itoyama, Toshiaki Takahashi, Masashi Aoki.
Abstract
Dysferlinopathies exhibit marked heterogeneity in the initial distribution of muscle involvement at the onset of the disease. We describe a Japanese patient with dysferlinopathy who exhibited distal anterior compartment myopathy (DACM) with early contractures of the ankle, whose pedigree included patients with two other types of dysferlinopathy. The existence of three phenotypes of dysferlinopathy in one pedigree is reported, indicating the involvement of molecules other than dysferlin in the pathogenesis.Entities:
Mesh:
Year: 2007 PMID: 17614318 DOI: 10.1002/mus.20836
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217