Pierre Robin sequence or syndrome is a genetic condition in which an infant is born with: -

• micrognathia (small jaw)
• glossoptysis (posterior/retracted tongue)
• cleft palate

As a result the infant may have breathing or feeding difficulties shortly after birth.

Initial management involves airway management and feeding support. Physiological effects usually resolve within 3–6 months however surgical repair may be indicated, particularly in cases which co-exist with a cleft palate. Most babies with Pierre Robin sequence will grow up to lead healthy adult lives.