Cataltepe S, Tuncbilek E
Department of Paediatrics, Hacettepe Medical School, Ankara, Turkey.
Eur J Pediatr. 1992 Apr;151(4):288-90. doi: 10.1007/BF02072231.
A 2-year-old boy with typical features of the acrocallosal syndrome is presented. His parents are first degree cousins and their first pregnancy resulted in spontaneous abortion whereas the offspring of their second pregnancy was an anencephalic baby with bilateral post-axial polydactyly of the hands. The possibility of including anencephaly in the spectrum of the CNS malformations of the acrocallosal syndrome is suggested.
本文报告了一名患有典型顶体胼胝体综合征的2岁男孩。他的父母是一级亲属,他们的第一次怀孕导致自然流产,而第二次怀孕的后代是一个无脑儿,双手双侧轴后多指畸形。本文提出将无脑儿纳入顶体胼胝体综合征中枢神经系统畸形谱的可能性。