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Abstract
Background: Recently, mutations in the transient receptor potential cation channel, subfamily V, member 4 gene (TRPV4) have been reported in Charcot-Marie-Tooth Type 2C (CMT2C) with vocal cord paresis. Other mutations in this same gene have been described in separate families with various skeletal dysplasias. Further clarification is needed of the different phenotypes associated with this gene.
Methods: We performed clinical evaluation, electrophysiology, and genetic analysis of the TRPV4 gene in 2 families with CMT2C.
Results: Two multigenerational families had a motor greater than sensory axonal neuropathy associated with variable vocal cord paresis. The vocal cord paresis varied from absent to severe, requiring permanent tracheotomy in 2 subjects. One family with mild neuropathy also manifested pronounced short stature, more than 2 SD below the average height for white Americans. There was one instance of dolichocephaly. A novel S542Y mutation in the TRPV4 gene was identified in this family. The other family had a more severe, progressive, motor neuropathy with sensory loss, but less remarkable short stature and an R315W mutation in TRPV4. Third cranial nerve involvement and sleep apnea occurred in one subject in each family.
Conclusion: CMT2C with axonal neuropathy, vocal cord paresis, and short stature is a unique syndrome associated with mutations in the TRPV4 gene. Mutations in TRPV4 can cause abnormalities in bone, peripheral nerve, or both and may result in highly variable orthopedic and neurologic phenotypes.
Footnotes
Study funding: Supported by the Department of Veterans Affairs, the Seattle Institute for Biomedical and Clinical Research, and the NIH (R01 NS069719).
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- CMAP
- compound muscle action potential
- CMT
- Charcot-Marie-Tooth
- CMT2C
- Charcot-Marie-Tooth Type 2C
- HMSN
- hereditary motor and sensory neuropathy
- NCV
- nerve conduction velocity
- RFLP
- restriction fragment length polymorphism
- SMA
- spinal muscular atrophy
- SNAP
- sensory nerve action potential
- SPSMA
- scapuloperoneal spinal muscular atrophy
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Supplemental data at www.neurology.org
- Received April 9, 2010.
- Accepted August 19, 2010.
- Copyright © 2010 by AAN Enterprises, Inc.
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