Pearn J
J Med Genet. 1978 Dec;15(6):409-13. doi: 10.1136/jmg.15.6.409.
A total population study of chronic childhood spinal muscular atrophy (arrested Werdnig-Hoffmann disease, Kugelberg-Welander disease, SMA type II and III) was undertaken in north-east England to establish gene and carrier frequencies, incidence, and prevalence. The incidence of this disease was 1 in 24 100 live births. Prevalence was 1.20 per 100,000 of the general population. A technique for estimating an autosomal recessive gene frequency in the known presence of dominant new mutations (or phenocopies), using data from a segregation analysis, is described. Gene frequency was in the range (0.00451 to 0.00659 (95% confidence limits), with a working estimate of 0.0055. Carrier rates for the autosomal recessive gene concerned were 1 in 76 to 1 in 111 (95%) confidence limits), with a working estimate of 1 in 90 for genetic counselling purposes.
在英格兰东北部对儿童慢性脊髓性肌萎缩症(静止型韦尼克 - 霍夫曼病、库格尔贝格 - 韦兰德病、II型和III型脊髓性肌萎缩症)进行了一项总体人群研究,以确定基因频率、携带者频率、发病率和患病率。该疾病的发病率为每24100例活产中有1例。普通人群中的患病率为每10万人中有1.20例。描述了一种利用分离分析数据在已知存在显性新突变(或表型模拟)的情况下估计常染色体隐性基因频率的技术。基因频率范围为(0.00451至0.00659(95%置信区间),有效估计值为0.0055。相关常染色体隐性基因的携带者比率为1/76至1/111(95%置信区间),出于遗传咨询目的的有效估计值为1/90。