Turkel S B, Ebbin A J, Towner J W
J Med Genet. 1983 Jun;20(3):227-9. doi: 10.1136/jmg.20.3.227.
A newborn female with intrauterine growth retardation, bilateral cleft lip and palate, absent external nares and eyelids, low set ears, short contracted limbs, webbed digits, intestinal malrotation, and unilateral renal agenesis is reported. These multiple malformations are considered part of the Neu-Laxova syndrome.
报告了一名患有宫内生长迟缓、双侧唇腭裂、无外鼻孔和眼睑、低位耳、肢体短缩、并指、肠旋转不良和单侧肾缺如的新生儿女性。这些多种畸形被认为是Neu-Laxova综合征的一部分。