Pierre Robin sequence: report of two cases

R J Hegde1, N R Mathrawala

  • 1Department of Pediatric and Preventive Dentistry, Bharati Vidyapeeth Deemed University Dental College and Hospital, Navi Mumbai, India. drrahulhegde@gmail.com

Insights

Pierre Robin sequence (PRS) is a congenital condition characterized by micrognathia, glossoptosis, and cleft palate. This study presents two cases where palatal obturators were used to address feeding difficulties in neonates with PRS.

Area of Science:

  • Craniofacial anomalies
  • Pediatric dentistry
  • Congenital malformations

Background:

  • Pierre Robin sequence (PRS) is a congenital condition resulting from first brachial arch malformation.
  • PRS is characterized by a triad of micrognathia (small jaw), glossoptosis (tongue falling back), and cleft palate.
  • Feeding difficulties are common in neonates diagnosed with PRS, particularly those with a complete cleft palate.

Observation:

  • Two cases of neonates diagnosed with Pierre Robin sequence are presented.
  • Both patients exhibited a complete cleft palate, contributing to feeding challenges.
  • The study focuses on the management of feeding issues in these infants.

Findings:

  • Palatal obturators were constructed for both neonates with PRS.
  • The construction of palatal obturators aimed to mitigate feeding problems associated with the condition.
  • This highlights a potential therapeutic approach for managing PRS-related feeding issues.

Implications:

  • Palatal obturators may offer a viable solution for improving feeding in infants with Pierre Robin sequence.
  • Early intervention with custom oral appliances can potentially improve nutritional intake and overall health outcomes.
  • Further research into the efficacy of palatal obturators in managing PRS is warranted.

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