Combarros O, Calleja J, Polo J M, Berciano J
Acta Neurol Scand. 1987 Jan;75(1):9-12. doi: 10.1111/j.1600-0404.1987.tb07882.x.
One hundred and forty-four patients with hereditary motor and sensory neuropathy (HMSN) were selected from within a defined area (Cantabria) in Northern Spain, from 1974 to 1984. The series comprises 49 index cases and 95 affected relatives. The prevalence ratio was 28.2 cases per 100,000. The results of the study indicate that the majority of the cases were hereditary as a dominant trait. The prevalence for the Type I HMSN cases did not differ from that of Type II cases. Previous population-surveys of these disorders are compared.
1974年至1984年间,从西班牙北部一个特定地区(坎塔布里亚)选取了144例遗传性运动和感觉神经病变(HMSN)患者。该系列包括49例索引病例和95例受影响的亲属。患病率为每10万人28.2例。研究结果表明,大多数病例为显性遗传特征。I型HMSN病例的患病率与II型病例无差异。并对以往这些疾病的人群调查进行了比较。