Nicholson G A
Department of Medicine, University of Sydney, Concord Hospital, Australia.
Neurology. 1991 Apr;41(4):547-52. doi: 10.1212/wnl.41.4.547.
The clinical expression of hereditary motor and sensory neuropathy type I (HMSN I) is age-dependent. Autosomal dominant HMSN I is heterogeneous at a molecular level with genes localized on chromosomes 1, 17, and possibly other chromosomes. In order to define accurately the penetrance of a single HMSN I gene mutation, we performed nerve conduction studies in HMSN I families whose genetic defect was linked to chromosome 17 (HMSN Ia). All HMSN Ia subjects tested had slow nerve conduction velocities with a mean median velocity 20 +/- 6 m/sec, which did not change with age. The range of conduction velocities from affected individuals did not overlap those from their clinically normal relatives, indicating complete penetrance of the gene from early childhood. The results indicate that motor nerve conduction studies in children can add additional information for linkage studies and genetic counseling.
遗传性运动和感觉神经病I型(HMSN I)的临床表现与年龄相关。常染色体显性遗传的HMSN I在分子水平上具有异质性,相关基因定位于1号、17号染色体,可能还有其他染色体。为了准确界定单个HMSN I基因突变的外显率,我们对遗传缺陷与17号染色体相关的HMSN I家系(HMSN Ia)进行了神经传导研究。所有接受检测的HMSN Ia受试者神经传导速度均较慢,正中神经平均传导速度为20±6米/秒,且不随年龄变化。患病个体的传导速度范围与临床正常亲属的传导速度范围没有重叠,这表明该基因从儿童早期就具有完全外显率。结果表明,儿童运动神经传导研究可为连锁研究和遗传咨询提供更多信息。