Pierre Robin syndrome-faciodigital anomaly syndrome

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.

Also known as: Chitayat-Meunier-Hodgkinson syndrome, Pierre Robin sequence-faciodigital anomaly syndrome, Chitayat Meunier Hodgkinson syndrome, Pierre Robin sequence with facial and digital anomalies, Pierre Robin syndrome, faciodigital anomaly, Robin sequence with facial and digital anomalies

0 clinical trials for this condition and its sub-types, 0 tagged with Pierre Robin syndrome-faciodigital anomaly syndrome itself.