Fryns J P, Snoeck L, Kleczkowska A, Van den Berghe H
Helv Paediatr Acta. 1985;40(6):485-8.
In this report a male newborn with Opitz trigonocephaly syndrome is described. In addition to the typical dysmorphic stigmata, terminal transverse limb reduction defects were observed. Acral limb deficiencies have not been previously reported to be associated with this multiple malformation syndrome.
本报告描述了一名患有Opitz三角头畸形综合征的男性新生儿。除了典型的畸形特征外,还观察到肢体末端横向发育不全缺陷。之前尚未报道过肢体末端缺陷与这种多发性畸形综合征相关。