PREVALENCE OF HEREDITARY MOTOR AND SENSORY NEUROPATHY IN CANTABRIA
PREVALENCE OF HEREDITARY MOTOR AND SENSORY NEUROPATHY IN CANTABRIA
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DOI：
10.1111/j.1600-0404.1987.tb07882.x
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发表时间：
1987-01-01
影响因子：
3.5
通讯作者：
BERCIANO, J
中科院分区：
文献类型：
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作者：
COMBARROS, O;CALLEJA, J;BERCIANO, J
1974 年至 1984 年间，从西班牙北部的一个特定地区（坎塔布里亚）选出了 144 名患有遗传性运动和感觉神经病 (HMSN) 的患者。该系列包括 49 名指示病例和 95 名受影响的亲属。患病率为每10万人28.2例。研究结果表明，大多数病例都是遗传性的显性特征。 I 型 HMSN 病例的患病率与 II 型病例没有差异。比较了以前对这些疾病的人口调查。
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.