McBrien Angela, Sands Andrew, Paterson Annie, Tharmaratnam Suresh, Thornton Claire
Department of Paediatric Cardiology, The Royal Belfast Hospital for Sick Children, Belfast, Northern Ireland, United Kingdom.
Fetal Pediatr Pathol. 2008;27(6):259-63. doi: 10.1080/15513810802448027.
We report a case of common arterial trunk with thanatophoric dysplasia. The skeletal dysplasia was diagnosed during fetal life. Following early induction of labour, there was a post-mortem diagnosis of type 2 common arterial trunk. This report includes the radiological and post-mortem findings. To our knowledge, thanatophoric dysplasia has never previously been reported in combination with any major cardiac defect.
我们报告一例合并致死性骨发育不全的共同动脉干病例。骨骼发育异常在胎儿期被诊断出来。在早期引产之后，尸检诊断为2型共同动脉干。本报告包括影像学和尸检结果。据我们所知，此前从未有过致死性骨发育不全合并任何主要心脏缺陷的报道。
