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

页码：103 / 114

页数：12