Article
Clinical phenotype, muscle MRI and muscle pathology of LGMD1F.
Journal of neurology - 1 Aug 2013
Peterle Enrico, Fanin Marina, Semplicini Claudio, Padilla Juan Jesus Vilchez, Nigro Vincenzo, Angelini Corrado
Abstract excerpt
Of the seven autosomal dominant genetically distinct forms of LGMD so far described, in only four the causative gene has been identified (LGMD1A-1D). We describe clinical, histopathological and muscle MRI features of a large Italo-Spanish kindred with LGMD1F presenting proximal-limb and axial muscle weakness. We obtained complete clinical data and graded the progression of the disease in 29 patients. Muscle MRI...
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