Chitayat Meunier Hodgkinson syndrome
Other Names: Robin sequence with facial and digital anomalies; Pierre Robin syndrome, faciodigital anomaly
This syndrome is characterised 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.
NIH genetic and rare disease info[edit source]
Chitayat Meunier Hodgkinson syndrome is a rare disease.
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