Recessive microtia, meatal atresia, and hearing loss. Report of a sibship.
Recessive microtia, meatal atresia, and hearing loss. Report of a sibship.
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隐性小耳症、耳道闭锁和听力损失。
DOI：
10.1001/archotol.1972.00770090179002
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发表时间：
1972
影响因子：
--
通讯作者：
H. Haskins
中科院分区：
文献类型：
--
作者：
B. Konigsmark;G. Nager;H. Haskins
两兄弟中的一个有双侧小耳畸形，另一个有单侧小耳畸形、外耳道闭锁和严重的听力障碍。耳廓重建中度成功。一个男孩的颞骨断层显示外耳道缺失，听小骨异常，中耳小。内耳正常。这些兄弟姐妹可能患有Ellwood等人在两个兄弟姐妹中描述的Reconciliated遗传综合征，其特征为小耳畸形、耳道闭锁和听力损失。
One of two brothers had bilateral and the other had unilateral microtia, meatal atresia, and significant hearing impairment. Reconstruction of the auricles was moderately successful. Temporal bone tomograms on one boy showed absent external canals, abnormal ossicles, and small middle ears. The inner ears were normal. These sibs probably have a recessively inherited syndrome described by Ellwood et al in two siblings and characterized by microtia, meatal atresia, and hearing loss.