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与耳前赘生物相关的听力障碍。

Hearing impairment in connection with preauricular tags.

作者信息

Kankkunen A, Thiringer K

出版信息

Acta Paediatr Scand. 1987 Jan;76(1):143-6. doi: 10.1111/j.1651-2227.1987.tb10431.x.

Abstract

Between 1977 and 1984, 230 newborns (5.4/1,000 livebirths) were registered at the two maternity hospitals of Göteborg as having preauricular tags. Of these 188 were available for hearing assessment. In 10 children (5%) the tag was associated with other malformations of the ear/face region. All these children had hearing impairment (HI), 8 conductive, 1 sensorineural and 1 mixed. In 178 neonates the tag was the only defect. Of these, 23 (13%) were found to have HI, all sensorineural and of mild to moderate degree. In the total group of children a positive family history for HI was found in 29% and for malformation in 24%. In the children where HI was found (33 cases in total) the figures for heredity rose to 67% (HI) and 30% (malformation). In the 23 cases with ear tag and HI, a hereditary tendency for HI was found to be 78%. Accordingly there is a clearly elevated risk for HI in connection with ear tags and we therefore recommend routine hearing assessment in all children with preauricular tags.

摘要

1977年至1984年间,哥德堡的两家妇产医院登记了230例患有耳前附器的新生儿(每1000例活产中有5.4例)。其中188例可进行听力评估。10名儿童(5%)的耳前附器与耳/面部区域的其他畸形有关。所有这些儿童都有听力障碍(HI),8例为传导性,1例为感音神经性,1例为混合性。178例新生儿中,耳前附器是唯一的缺陷。其中,23例(13%)被发现有HI,均为感音神经性,程度为轻度至中度。在所有儿童中,29%有HI家族史,24%有畸形家族史。在发现有HI的儿童(共33例)中,遗传率分别升至67%(HI)和30%(畸形)。在23例有耳前附器且有HI的病例中,HI的遗传倾向为78%。因此,与耳前附器相关的HI风险明显升高,因此我们建议对所有患有耳前附器的儿童进行常规听力评估。

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