Pierre Robin syndrome-faciodigital anomaly syndrome
Findings
No curated finding names Pierre Robin syndrome-faciodigital anomaly syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0010710), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
2 names
Resolves to: Pierre Robin syndrome-faciodigital anomaly syndrome
- Also called
- Chitayat-Meunier-Hodgkinson syndromePierre Robin sequence-faciodigital anomaly syndrome