Isolated Pierre-Robin syndrome
MONDO:0009869Pierre-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
8 clinical trials for this condition and its sub-types.
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Broader categories
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Massive study seeks clues to facial differences
Knowledge-focused Recruiting nowThis study aims to learn more about abnormal development of the face, head, and neck by comparing people with these conditions to their family members and healthy volunteers. Researchers will collect medical history, perform exams, take 3D images, and analyze genetic samples from…
Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused
Last updated Aug 30, 2026 00:00 UTC
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Massive database aims to unlock secrets of facial birth defects
Knowledge-focused Recruiting nowThis study is creating a large database of genetic and physical information from 3100 children with craniofacial abnormalities, such as craniosynostosis and Pierre Robin sequence. Researchers will analyze this data to understand why these conditions vary so much from person to pe…
Sponsor: Imagine Institute • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:07 UTC