Neuropathy as a presenting feature in fragile X-associated tremor/ataxia syndrome

被引:42
作者
Hagerman, Randi J.
Coffey, Sarah M.
Maselli, Ricardo
Soontarapornchai, Kultida
Brunberg, James A.
Lechey, Maureen A.
Zhang, Lin
Gane, Louise W.
Fenton-Farrell, Grace
Tassone, Flora
Hagerman, Paul J.
机构
[1] Univ Calif Davis, Davis Hlth Syst, MIND Inst, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Med Ctr, Dept Pediat, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Sch Med, Dept Neurol, Sacramento, CA 95817 USA
[4] Univ Calif Davis, Med Ctr, Dept Radiol, Sacramento, CA 95817 USA
[5] Univ Colorado, Hlth Sci Ctr, Dept Neurol, Denver, CO 80202 USA
[6] Univ Calif Davis, Sch Med, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
关键词
fragile X-associated tremor/ataxia syndrome; neuropathy; fragile X; tremor; ataxia; FMR1;
D O I
10.1002/ajmg.a.31920
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Peripheral neuropathy is common among patients with fragile X-associated tremor ataxia syndrome (FXTAS). Four patients with FXTAS are described with neuropathy as the presenting feature, two having received a prior diagnosis of Charcot-Marie-Tooth (CMT) disease. A fifth is described with neuropathy as the only clinical feature. A functional connection between FXTAS and neuropathy has been suggested by the presence of lamin A/C in the intranuclear, neuronal and astrocytic inclusions of FXTAS, since mutations in Iamin A/C are known to give rise to an axonal form of CMT. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:2256 / 2260
页数:5
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