轴后性肢端面部发育不全或米勒综合征。病例报告。
Postaxial acrofacial dysostosis or Miller syndrome. A case report.
作者信息
Barbuti D, Orazi C, Reale A, Paradisi C
机构信息
Department of Radiology, Ospedale Bambino Gesu, Roma, Italy.
出版信息
Eur J Pediatr. 1989 Feb;148(5):445-6. doi: 10.1007/BF00595909.
PMID:2920751
Abstract
A case of postaxial acrofacial dysostosis (Miller syndrome) is presented. This rare syndrome is essentially characterized by a Treacher-Collins-like facial appearance together with absence of the fifth digital ray of all limbs and variable forearm hypoplasia.
摘要
本文报告1例轴后性肢端面部发育不全（米勒综合征）。这种罕见综合征的基本特征是具有类似特雷彻·柯林斯综合征的面部外观，同时所有四肢均无第五指骨射线，且前臂发育不全程度不一。
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