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

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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Bibliographic Details
Main Authors: A-ping Sun, Lu Tang, Qin Liao, Hui Zhang, Ying-shuang Zhang, Jun Zhang
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Neural Regeneration Research
Subjects:
nerve regeneration; PMP22 duplication; demyelinating degeneration; hereditary disease; phenotype; axonal loss; electrophysiology; concentric structure; multiplex ligation-dependent probe amplification; neural regeneration
Online Access:http://www.nrronline.org/article.asp?issn=1673-5374;year=2015;volume=10;issue=10;spage=1696;epage=1699;aulast=Sun

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http://www.nrronline.org/article.asp?issn=1673-5374;year=2015;volume=10;issue=10;spage=1696;epage=1699;aulast=Sun

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