Ruev P, Dakov D, Mumdzhiev Kh, Buzalov S
Akush Ginekol (Sofiia). 2004;43(4):56-60.
Implementation of Central Registry for hearing loss in children can answer many questions about the frequency, etiology and habilitation of hearing impairment by infant. Precondition for realize is implementation of universal newborn hearing screening. With introduction this screening we decrease dramatically the age of children, of which we predict, diagnosed and intervened bilaterally hearing loss. Despite the progress of the medicine, in particularly of the genetic, the etiology of some cases with hearing loss stay unknown. Future investigations in this field, inclusive molecular-genetic, is necessary to determine hereditary hearing loss by children in Bulgaria.
实施儿童听力损失中央登记系统可以回答许多关于婴儿听力障碍的发生率、病因和康复情况的问题。实现这一目标的前提是实施普遍的新生儿听力筛查。随着这种筛查的引入,我们大大降低了那些我们预测、诊断和干预双侧听力损失儿童的年龄。尽管医学取得了进步,尤其是遗传学方面,但一些听力损失病例的病因仍然不明。该领域未来的研究,包括分子遗传学研究,对于确定保加利亚儿童的遗传性听力损失是必要的。