Plöchl E, Tasser C
Padiatr Padol. 1980;15(4):375-84.
This is a report on 104 children with bilateral sensorineural deafness at an institute for children with hearing defects. The children were analyzed etiologically, familial genetic cases are predominant and even in the group of hearing defects of unknown cause, there are surely those where in fact a genetic defect just remained undetected. Hearing defects following rubella during pregnancy will become rare as rubella prophylaxis continues to grow more widespread. Similarly, other prenatal and perinatal causes can also be expected to become less common now that prenatal check-ups are more prevalent and perinatology is achieving the success it is. For this very reason too, deafness following hyperbilirubinemia in a new-born baby is becoming less frequent. Ototoxic drugs must be continued to be avoided especially in combined use and in view of the probable increase in familial genetic cases, human genetic counselling must be propagated as well emphasis laid on early detection and early treatment.
这是一份关于一所听力缺陷儿童研究所中104例双侧感音神经性耳聋患儿的报告。对这些患儿进行了病因分析,发现家族遗传病例占主导地位,即使在病因不明的听力缺陷组中,肯定也有一些实际上是遗传缺陷但未被检测到的情况。随着风疹预防措施越来越广泛,孕期感染风疹后导致的听力缺陷将变得罕见。同样,鉴于产前检查更加普及且围产医学取得了现在这样的成功,其他产前和围产期原因预计也会变得不那么常见。正因为如此,新生儿高胆红素血症后导致的耳聋也越来越少。必须继续避免使用耳毒性药物,尤其是联合使用时,而且鉴于家族遗传病例可能增加,还必须推广人类遗传咨询,并强调早期发现和早期治疗。