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Isolated Pierre-Robin syndrome
rarePierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft.
- Identifiers
- MONDO:0009869 OMIM:261800Orphanet:718
- Part of
- Eye disorder
- Also known as
- glossoptosis, micrognathia, and cleft palate · isolated Pierre Robin sequence · Pierre Robin Sequence · Pierre Robin syndrome skeletal dysplasia polydactyly
Subtypes
| Disease | Subtypes |
|---|---|
| Radial defect robin sequence |
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