Rare syndromes in dentistry Part 1: The Pierre Robin sequence: a focus on a rare congenital anomaly

Authors

  • P Cascone Full Professor of Maxillofacial Surgery, UniCamillus International University of Health Sciences, Rome
  • V Quinzi Department of Life, Health & Environmental Sciences, Postgraduate School of Orthodontics, University of L'Aquila, L'Aquila
  • F Maffìa Maxillofacial Surgery Unit, Department of Neurosciences, Reproductive and Odontostomatological Sciences, "Federico II" University of Naples, Naples
  • E Trebbi Department of Infectious Diseases and Public Health, "La Sapienza" University of Rome, Rome, Italy - Research Student Programme "Studenti per la Ricerca", UniCamillus International University of Health Sciences
  • G Marzo Department of Life, Health & Environmental Sciences, Postgraduate School of Orthodontics, University of L'Aquila, L'Aquila

DOI:

https://doi.org/10.23804/ejpd.2023.24.01.14

Keywords:

Mandibular Osteodistraction, Micrognathia, Pierre Robin Sequence, Congenital Anomalies

Abstract

AIM: The aim of this paper was to enlighten the peculiar findings of the Pierre Robin sequence, a rare congenital anomaly with important afterbirth comorbidities. The management of this pathology requires highly specialised centers and highly qualified specialists in order to offer the best therapeutic strategy to the affected child. Early diagnosis and parental counseling play a key role in the managing of PRS: an earlier activation of the treatment path helps to yield better outcomes and to prevent complications. A case of a newborn affected by PRS is presented, showing the steps of the treatment strategy and the final outcome.

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