Marazita M L, Ploughman L M, Rawlings B, Remington E, Arnos K S, Nance W E
Department of Human Genetics, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0003.
Am J Med Genet. 1993 Jun 15;46(5):486-91. doi: 10.1002/ajmg.1320460504.
Profound, early-onset deafness is present in 4-11 per 10,000 children, and is attributable to genetic causes in at least 50% of cases. Family history questionnaires were sent to 26,152 families of children with profound, early-onset deafness not known to be related to an environmental cause. The probands were ascertained through the 1988-89 Gallaudet University Annual Survey of Hearing Impaired Children and Youth. The analysis is based on the responses that were received from 8,756 families. Classical segregation analysis was used to analyze the family data, and to estimate the proportions of sporadic, recessive and dominant causes of deafness in the families. These data were consistent with 37.2% of the cases due to sporadic causes, and 62.8% due to genetic causes (47.1% recessive, and 15.7% dominant). An earlier study using the 1969-70 Annual Survey found 49.3% sporadic cases and 50.6% genetic, demonstrating that the proportion of sporadic cases of early-onset deafness has significantly decreased since 1970.
每10000名儿童中,有4至11名患有严重的早发性耳聋,其中至少50%的病例可归因于遗传因素。研究人员向26152名患有严重早发性耳聋且病因不明与环境因素无关的儿童家庭发放了家族史调查问卷。这些先证者是通过1988 - 1989年加劳德特大学听力受损儿童和青少年年度调查确定的。分析基于从8756个家庭收到的回复。采用经典分离分析法对家庭数据进行分析,以估计家庭中散发性、隐性和显性耳聋病因的比例。这些数据表明,37.2%的病例是由散发性原因引起的,62.8%是由遗传原因引起的(47.1%为隐性遗传,15.7%为显性遗传)。一项早期使用1969 - 1970年年度调查的研究发现,散发性病例占49.3%,遗传病例占50.6%,这表明自1970年以来,早发性耳聋散发性病例的比例显著下降。