CHOANAL ATRESIA AND ASSOCIATED MULTIPLE ANOMALIES
CHOANAL ATRESIA AND ASSOCIATED MULTIPLE ANOMALIES
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DOI：
10.1016/s0022-3476(79)80513-2
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发表时间：
1979-01-01
影响因子：
5.1
通讯作者：
HALL, BD
中科院分区：
文献类型：
--
作者：
HALL, BD
通过后鼻孔闭锁的存在来识别具有未知病因的多种异常的无关患者[17]。确定了相关特征的定期复发模式，包括智力低下、出生后生长缺陷、生殖器发育不良（男性）、小耳、心脏缺陷、小颌、出生后小头畸形和眼缺损。后鼻孔闭锁伴发不明原因的多发性畸形时，预后严重，可预测的相关缺陷模式。
Unrelated patients [17] with multiple anomalies of unknown etiology were identified by the presence of choanal atresia. A regularly recurring pattern of associated features involving mental retardation, postnatal growth deficiency, hypogenitalism (males), small ears, cardiac defects, micrognathia, postnatal microcephaly and ocular coloboma was identified. Choanal atresia when accompanied by multiple anomalies of unknown etiology has a serious prognosis with a predictable pattern of associated defects.