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Figure 2 | BMC Medical Genetics

Figure 2

From: Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for “double trouble” overlapping syndromes

Figure 2

Family history. The patient’s parents died early and had no symptoms of muscle weakness or neuropathy. Neither did the mother’s four siblings and their progenies. Besides our patient one of his sisters and her older daughter show similar symptoms of peripheral neuropathy with foot deformities and gait difficulties. No symptoms of muscle wasting or weakness occurred in these two family members until now.

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