{Reference Type}: Journal Article
{Title}: Syndromic Piere Robbin Sequence- A Rare Presentation in Association with Multiple Heart Defects and Type III Stickler Syndrome.
{Author}: Akhtar S;Wasif M;Afzal Y;Shahab I;Dhanani R;Shaikh AR;
{Journal}: Indian J Otolaryngol Head Neck Surg
{Volume}: 76
{Issue}: 1
{Year}: 2024 Feb
暂无{DOI}: 10.1007/s12070-023-04307-x
{Abstract}: 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.