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Fig. 1 | BMC Neurology

Fig. 1

From: A TRPV4 mutation caused Charcot-Marie-Tooth disease type 2C with scapuloperoneal muscular atrophy overlap syndrome and scapuloperoneal spinal muscular atrophy in one family: a case report and literature review

Fig. 1

Clinical and MRI findings of patient 1. The patient exhibited scapular muscle atrophy, resulting in sloping shoulders (A), as well as significant atrophy of hand intrinsic muscles (B) and calf muscles (C). MRI revealed atrophy of the thigh (D) and calf (E) muscles with concurrent fat infiltration. The brachial plexus was hypertrophy and hyperintense (F)

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BMC Neurology

ISSN: 1471-2377

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