%0 Journal Article
%T Syndromic Piere Robbin Sequence- A Rare Presentation in Association with Multiple Heart Defects and Type III Stickler Syndrome.
%A Akhtar S
%A Wasif M
%A Afzal Y
%A Shahab I
%A Dhanani R
%A Shaikh AR
%J Indian J Otolaryngol Head Neck Surg
%V 76
%N 1
%D 2024 Feb
%M 38440550
暂无%R 10.1007/s12070-023-04307-x
%X 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.