Labrune P, Trioche P, Fallet-Bianco C, Roume J, Narcy F, Le Merrer M
Service de Pédiatrie, Hôpital Antoine Béclère, Clamart, France.
Am J Med Genet. 1997 Dec 12;73(2):144-9.
Six fetuses with normal chromosomes were found to have severe craniofacial, limb, and visceral malformations during the second trimester of pregnancy. Two of these fetuses were monozygotic twins while a third one had a healthy dizygotic twin brother. A case with familial recurrence was also observed. Autopsy and skeletal radiographs suggested several diagnoses such as neural tube defect with limb defects or XK aprosencephaly. The development of these severe conditions in monozygotic twins and familial recurrence emphasize the difficulties of genetic counseling in such situations. These cases may suggest autosomal recessive inheritance.
在妊娠中期发现6例染色体正常的胎儿存在严重的颅面、肢体和内脏畸形。其中2例胎儿为单卵双胞胎,另一例有一个健康的双卵双胞胎兄弟。还观察到1例有家族复发情况。尸检和骨骼X光片提示了几种诊断,如伴有肢体缺陷的神经管缺陷或无脑回畸形。单卵双胞胎中这些严重病症的发生以及家族复发情况凸显了在此类情况下进行遗传咨询的困难。这些病例可能提示常染色体隐性遗传。