Menashi M, Ornoy A, Cohen M M
Teratology. 1977 Jun;15(3):325-8. doi: 10.1002/tera.1420150315.
A fetus of 20 to 21 weeks of development with the trisomy 18 syndrome has been described. In addition to the phenotypic manifestations usually associated with the syndrome, i.e., low set ears, short neck, omphalocoele, flexion of fingers with the convergence of the second and fifth digits, rocker bottom feet, urinary tract anomalies and intrauterine growth retardation, the fetus also showed left diaphragmatic hernia. Anencephaly and aplasia of the squamous part of occipital bone. Since anencephaly has never been described as one of the phenotypic manifestations of trisomy 18, it is reasonable to assume that in the present fetus it is unrelated and resulted from secondary destruction of the neural tube.
已描述了一名发育20至21周、患有18三体综合征的胎儿。除了通常与该综合征相关的表型表现,即低位耳、短颈、脐膨出、手指屈曲且第二和第五指并拢、摇椅底足、泌尿系统异常和宫内生长迟缓外,该胎儿还表现出左侧膈疝、无脑儿和枕骨鳞状部发育不全。由于无脑儿从未被描述为18三体综合征的表型表现之一,因此有理由推测在当前胎儿中,它与该综合征无关,而是神经管继发性破坏所致。