Cochlear implantation in a patient with deafness induced by Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathies).

Abstract

Charcot-Marie-Tooth disease (CMT), also named hereditary motor and sensory neuropathies (HMSN), comprises a clinically and genetically heterogeneous group of disorders affecting the peripheral nervous system. Deafness induced by CMT is clinically distinct among the genetically heterogeneous group of CMT disorders. Deafness in CMT patients is associated with point mutations or deletions in the transmembrane domain in the peripheral myelin gene (PMP) 22, which are in close proximity to the extracellular component of this gene. We present a patient with deafness induced by CMT type 1A, undergoing cochlear implantation. Prior investigations showed good results due to replacing a synchronous impulse by means of cochlear implantation in patients with auditory neuropathy.

• Authors: J T F Postelmans, R J Stokroos
• Journal: The Journal of laryngology and otology (J Laryngol Otol) Vol. 120 Issue 6 Pg. 508-10 (Jun 2006) ISSN: 0022-2151 [Print] England
• PMID: 16772060 (Publication Type: Case Reports, Journal Article, Review)

Chemical References

• Myelin Proteins
• PMP22 protein, human

Topics

• Charcot-Marie-Tooth Disease (complications, genetics, surgery)
• Cochlear Implantation
• Female
• Hearing Loss, Sensorineural (etiology, genetics, surgery)
• Humans
• Middle Aged
• Myelin Proteins (genetics)
• Point Mutation
• Treatment Outcome