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ARTICLE
Year : 2007  |  Volume : 12  |  Issue : 1  |  Page : 35-38

ChaRcot-Marie-Tooth disease presenting in a young Nigerian male: A case report


Department of Medicine, University of Nigeria Teaching Hospital, Enugu, Nigeria

Correspondence Address:
MBBS FWACP I O Onwuekwe
Department of Medicine, University of Nigeria Teaching Hospital, P.M.B. 1129, Enugu
Nigeria
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Source of Support: None, Conflict of Interest: None


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Background: Charcot-Marie-Tooth disease is a heterogeneous group of inherited peripheral neuropathy. It has various genetic and phenotypic characteristics and can be a significant cause of morbidity with severe disabling consequences. Often the diagnosis may be missed. It is not commonly encountered in Nigerian medical clinics and there is no documented prevalence rate for the country. Method: A case report of a 31-year-old man presenting to the medical outpatient clinic of the University of Nigeria Teaching Hospital Enugu with features of Charcot -Marie - Tooth disease is presented. Relevant literature is also reviewed. Result: A thirty three year old Nigerian male presented to the medical clinic with a thirteen-year history of progressive paraesthesiae in the feet, which later involved the hands. This was accompanied seven years later by gradual onset weakness of the muscles especially the distal group in both upper and lower limbs which led to paralysis. No sphincter involvement. Family history was not contributory. He had typical features of HMSN type I and was a possible proband. Conclusion: Though not common, the inherited peripheral neuropathies are a cause of significant morbidity. When recognized there are potential issues of genetic counseling that arise for which Nigerians are yet to come to terms with.


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