Pierre Robin Sequence is a congenital condition characterized by a combination of three main features: a small jaw (micrognathia), a tongue that is positioned further back in the throat (glossoptosis), and a cleft palate. These features can lead to breathing difficulties, feeding challenges, and other complications in newborns. The exact cause of Pierre Robin Sequence is not always clear, but it can occur as an isolated condition or as part of other syndromes. Early diagnosis and intervention, including feeding support and potential surgical options, are important for managing the symptoms and improving the quality of life for affected infants.