Coexistent Charcot-Marie-Tooth type 1A and type 2 diabetes mellitus neuropathies in a Chinese family

Charcot-Marie-Tooth disease type 1A (CMT1A) is caused by duplication of the peripheral myelin protein 22 (PMP22) gene on chromosome 17. It is the most common inherited demyelinating neuropathy. Type 2 diabetes mellitus is a common metabolic disorder that frequently causes predominantly sensory neuro...

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Detalles Bibliográficos
Autores principales: Sun, A-ping, Tang, Lu, Liao, Qin, Zhang, Hui, Zhang, Ying-shuang, Zhang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Special Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660768/
https://www.ncbi.nlm.nih.gov/pubmed/26692872
http://dx.doi.org/10.4103/1673-5374.167771

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660768/
https://www.ncbi.nlm.nih.gov/pubmed/26692872
http://dx.doi.org/10.4103/1673-5374.167771

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