患有颌面部发育异常综合征（无颌-耳头畸形）胎儿的计算机断层扫描重建图像。
Computed tomographic reconstruction of a fetus with the dysgnathia complex (agnathia-otocephaly).
作者信息
Rajan Priya V, Wing Deborah A, Bocian Maureen, McKeown Anna
机构信息
Department of Obstetrics and Gynecology, University of California Irvine Medical Center, 101 The City Drive, Building 56, Suite 800, Orange, CA 92868, USA.
出版信息
Prenat Diagn. 2007 Feb;27(2):130-2. doi: 10.1002/pd.1626.
The dysgnathia complex (agnathia-otocephaly) (AO) is a lethal malformation that consists of congenital absence of the lower jaw with union or close approximation of the lower ears on the front of the neck, microstomia, and hypoglossia. We present a novel case of agnathia-otocephaly with associated organomegaly and the use of postmortem 3-D computed tomographic rendering.
颌面部发育不全综合征（无颌-耳-头畸形）（AO）是一种致死性畸形，其特征包括先天性下颌骨缺失、颈部前方低位耳融合或紧密靠近、小口畸形和舌发育不全。我们报告一例伴有器官肿大的无颌-耳-头畸形新病例，并介绍了尸检三维计算机断层扫描成像技术的应用。
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