Feinmesser M, Tell L, Levi H
Department of Otolaryngology and Speech and Hearing Center, Hadassah University Hospital, Jerusalem, Israel.
Audiology. 1989;28(5):268-71. doi: 10.3109/00206098909081633.
A longitudinal study was performed on Jewish children with moderately-severe to profound hearing impairment born in Jerusalem during a period of 15 years (1967-1982), and the data on consanguineous matings among their parents were analyzed. These data were estimated in relation to the records obtained in an earlier survey performed on Jewish deaf children during the years 1955-1964. The rate of consanguinity among the parents of hearing-impaired children was much lower in the present survey than in the earlier one in both the Ashkenazi (Central and Eastern European origin) and the non-Ashkenazi (Asian-African origin) group. It is assumed that there is a better understanding of the genetic risk in consanguineous unions, especially when a disability such as hereditary deafness is involved.
对1967年至1982年期间在耶路撒冷出生的患有中度至重度或极重度听力障碍的犹太儿童进行了一项纵向研究,并分析了其父母近亲通婚的数据。这些数据是根据1955年至1964年期间对犹太聋哑儿童进行的早期调查记录估算得出的。在本次调查中,无论是德系犹太人(中欧和东欧血统)组还是非德系犹太人(亚非血统)组,听力障碍儿童父母的近亲结婚率均远低于早期调查。据推测,人们对近亲结合的遗传风险有了更好的认识,尤其是在涉及遗传性耳聋等残疾的情况下。