This syndrome is characterized by the association of Pierre Robin sequence (retrognathia, cleft palate and glossoptosis) with facial dysmorphism (high forehead with frontal bossing) and digital anomalies (tapering fingers, hyperconvex nails, clinodactyly of the fifth fingers and short distal phalanges, finger-like thumbs and easily subluxated first metacarpophalangeal joints).Growth and mental development were normal. The disease is Pierre Robin syndrome-faciodigital anomaly syndrome (Monarch Disease Ontology identifier MONDO_0010710). Also known as: Chitayat-Meunier-Hodgkinson syndrome, Pierre Robin sequence-faciodigital anomaly syndrome.