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. 2014 Oct 14;83(16):1453–1463. doi: 10.1212/WNL.0000000000000892

Figure 3. Diagnostic approach to patients with a limb-girdle pattern of weakness and suspected muscular dystrophy with an autosomal dominant inheritance pattern.

Figure 3

*Autosomal dominant, autosomal recessive, or X-linked inheritance may be responsible in sporadic cases. EDMD = Emery-Dreifuss muscular dystrophy; hIBMPFD = hereditary inclusion body myopathy with Paget disease and frontotemporal dementia; LGMD = limb-girdle muscular dystrophy; VCP = valosin-containing protein.