Isolated Pierre-Robin syndrome

MONDO:0009869

Pierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft.

Also known as: Pierre Robin Sequence, isolated Pierre Robin sequence, Pierre Robin syndrome skeletal dysplasia polydactyly, glossoptosis, micrognathia, and cleft palate

16 clinical trials for this condition and its sub-types.

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