[特雷彻-柯林斯综合征（作者译）]
[Treacher-Collins-syndrome (author's transl)].
作者信息
Schober E, Götz M, Scheibenreiter S
出版信息
Monatsschr Kinderheilkd (1902). 1977 Nov;125(11):938-70.
PMID:593281
Abstract
The Treacher-Collins syndrome is characterised by an anti-mongoloid slant of the eyes, hypoplasia of the facial bones, in particular the the mandible, and malformations of the external and middle ear with hearing loss. Early diagnosis of hearing defects is of prime importance as nowadays suitable treatment can prevent the resulting delay in speech development and secondary intellectual retardation.
摘要
特雷彻-柯林斯综合征的特征为眼睛呈反蒙古人种斜度、面部骨骼发育不全，尤其是下颌骨，以及外耳和中耳畸形并伴有听力丧失。听力缺陷的早期诊断至关重要，因为如今合适的治疗可预防由此导致的语言发育延迟和继发性智力发育迟缓。
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