皮埃尔·罗宾序列（PRS），一种罕见的先天性疾病,是小颌畸形的三合会,舌下垂，和舌源性气道阻塞（TBSO）。它可能是孤立异常（iPRS）或综合征（sPRS）的一部分，就像斯蒂克勒综合症一样。大约20%的PRS患儿患有先天性心脏病。据我们所知，这种一天大的婴儿病例是第一个被报道有两个心脏缺陷的病例；PierreRobbinSequence儿童的动脉导管未闭和卵圆孔未闭。
Pierre Robin Sequence (PRS), a rare congenital disorder, is a triad of micrognathia, glossoptosis, and tongue based airway obstruction (TBSO). It may occur as isolated anomaly (iPRS) or as a part of a syndrome (sPRS), like that seen in association with Stickler Syndrome. Approximately 20% of children with PRS have congenital heart diseases. To the best of our knowledge this case of a one-day old infant is the first one to be reported as having two heart defects; patent ductus arteriosus and patent foramen ovale in Pierre Robbin Sequence child.
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