A case report of peroneal muscle atrophy type 2A2 with central nervous system involvement as initial presentation
Abstract Background Charcot-Marie-Tooth disease (CMT) is a group of single-gene hereditary diseases of peripheral nerve with high clinical variability and genetic heterogeneity. The typical clinical manifestations include progressive muscle weakness and muscle atrophy in the distal extremities, acco...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2024-01-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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