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. 2013 Dec;19(6 Muscle Disease):1509–1534. doi: 10.1212/01.CON.0000440658.03557.f1

Figure 1-3.

Figure 1-3.

An 8-year-old boy with merosin-deficient congenital muscular dystrophy confirmed by DNA mutation analysis, which revealed a mutation of the LAMA 2 gene. A, Evidence of bilateral ptosis and facial weakness; B, severe dextroscoliosis and the presence of a gastrostomy tube; C, hyperlordosis and contractures at the elbow and wrist.