Haberlová J, Claeys K G, De Jonghe P, Seeman P
DNA laboratory, Department of Child Neurology, Second School of Medicine, Charles University Prague, 15200 Prague 5, Czech Republic.
Neuromuscul Disord. 2009 Jun;19(6):427-8. doi: 10.1016/j.nmd.2009.03.005. Epub 2009 May 5.
Distal hereditary motor neuropathy is a heterogeneous group of disorders characterised by a pure motor axonal neuropathy. It is occasionally associated with additional signs such as facial weakness, vocal cord paralysis, weakness of the diaphragm, and pyramidal signs. Although predominantly the inheritance is autosomal dominant, all types of inheritance have been described. Here we report a Czech family with cranial nerves palsy as an initial feature of a non progressive infantile onset dominant distal hereditary motor neuropathy. This family may represent a new subtype of distal hereditary motor neuropathy.
远端遗传性运动神经病是一组异质性疾病,其特征为纯运动性轴索性神经病。它偶尔会伴有其他体征,如面部无力、声带麻痹、膈肌无力和锥体束征。虽然主要遗传方式为常染色体显性遗传,但已描述了所有类型的遗传方式。在此,我们报告一个捷克家族,其以颅神经麻痹作为非进行性婴儿期起病的显性远端遗传性运动神经病的初始特征。这个家族可能代表了远端遗传性运动神经病的一种新亚型。