Clinical Associate Professor Stanford University / Lucile Packard Children's Hospital Stanford Stanford, California
Pierre Robin Sequence consists of a clinical triad of congenital micrognathia, glossoptosis and airway obstruction with or without cleft palate. The phenotypic presentation and complexity of this condition vary greatly and therefore it requires a multidisciplinary approach to management. Understanding the perinatal needs as well as treatment options is paramount in long-term success of patients with this condition.
Learning Objectives:
At the conclusion of this presentation, participants should be able to:
Examine perinatal care of infants born with Robin Sequence.
Discuss surgical and non-surgical treatment options for Robin Sequence.
Evaluate long-term outcomes and growth in patients with Robin Sequence.
