Sleep and Memory Disorders in a Patient Suffering from Charcot-Marie-Tooth Disease

Currently incurable, Charcot-Marie-Tooth (CMT) disease is the most commonly inherited neurological disorder, which affects a small percentage of the population. The most common cause of CMT is the duplication of a region on the short arm of chromosome 17, which includes the gene PMP22. We report a t...

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Detalles Bibliográficos
Autores principales: FLORESCU, C., ALBU, C.V., DUMITRESCU, C., TÂRTEA, G.C., FLORESCU, O.A., TÂRTEA, E.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medical University Publishing House Craiova 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286719/
https://www.ncbi.nlm.nih.gov/pubmed/30595858
http://dx.doi.org/10.12865/CHSJ.43.01.11
Descripción
Sumario:Currently incurable, Charcot-Marie-Tooth (CMT) disease is the most commonly inherited neurological disorder, which affects a small percentage of the population. The most common cause of CMT is the duplication of a region on the short arm of chromosome 17, which includes the gene PMP22. We report a thirty-seven-year-old man with CMT disease having sleep, memory and attention disorders characterized by brief retrograde amnesia at early age. The patient has no genetic disease in the family, but was diagnosed with diabetes mellitus, which emphasizes the sensory loss and prolonged infections. Diabetes mellitus emphasizes the sensory symptomatology and predisposes to the development of infections with delayed healing.

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