A large family with Charcot-Marie-Tooth Type 1A and Type 2 diabetes mellitus

被引：13
|
作者：
Koç, F [1 ]
Sarica, Y
Yerdelen, D
Baris, I
Battaloglu, E
Sert, M
机构：
[1] Cukurova Univ, Sch Med, Dept Neurol, Adana, Turkey
[2] Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
[3] Cukurova Univ, Sch Med, Dept Internal Med, Endocrinol Div, Adana, Turkey
来源：
INTERNATIONAL JOURNAL OF NEUROSCIENCE | 2006年 / 116卷 / 02期
关键词：
Charcot-Marie-Tooth disease Type 1A; duplication at chromosome 17p11.2; Type 2 diabetes mellitus;
D O I：
10.1080/00207450500341431
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
Charcot-Marie-Tooth (CMT) disease is a hereditary demyelinating peripheral neuropathy, and CMT Type 1A is the most common form. In most cases, CMT1A is usually caused by duplication at chromosome 17p11.2-12. Type 2 diabetes mellitus ( Type 2 DM) is a common metabolic disorder, characterized by chronic hyperglycemia that can be associated with micro- and/or macrovascular.
引用
收藏
页码：103 / 114
页数：12
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