Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24

被引:19
|
作者
McEntagart, ME
Reid, SL
Irtthum, A
Douglas, JB
Eyre, KED
Donaghy, MJ
Anderson, NE
Rahman, N
机构
[1] St George Hosp, Sch Med, Dept Med Genet, London SW17 0RE, England
[2] Inst Canc Res, Sect Canc Genet, Sutton, Surrey, England
[3] Auckland Hosp, Dept Neurol, Auckland, New Zealand
[4] Univ Oxford, Radcliffe Infirm, Dept Clin Neurol, Oxford OX2 6HE, England
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D O I
10.1002/ana.20375
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Hereditary motor and sensory neuropathy type IIC (HMSN IIC) is an autosomal dominant axonal neuropathy. The cardinal features include distal muscle wasting and weakness, vocal cord paralysis, and mild sensory impairment. Recently, HMSN IIC locus was mapped to chromosome 12q23-24. Two families affected by HMSN IIC were identified and evaluated for linkage to this region. Segregation analysis in both families was consistent with linkage to chromosome 12q23-24. Combined analysis generated a multipoint LOD score of 2.1 at marker D12S1583 and refined the HMSN IIC gene interval to The clinical and molecular findings are discussed.
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页码:293 / 297
页数:5
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