GTR Home > Conditions/Phenotypes > Robin sequence

Summary

Pierre Robin sequence is a craniofacial anomaly comprising mandibular hypoplasia, cleft secondary palate, and glossoptosis leading to life-threatening obstructive apnea and feeding difficulaties during the neonatal period (summary by Tan et al., 2013). [from OMIM]

Available tests

1 test is in the database for this condition.

Check Related conditions for additional relevant tests.

Associated cytogenetic location

  • Location: 17q24.3-q25.1

Clinical features

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