A case of Pierre Robin syndrome in a child with no soft palate and complications from pneumonia in Bangladesh
- PMID: 37205152
- PMCID: PMC10185733
- DOI: 10.1002/ccr3.7350
A case of Pierre Robin syndrome in a child with no soft palate and complications from pneumonia in Bangladesh
Abstract
Key clinical message: Children with Pierre Robin syndrome (PRS) often have trouble breathing and eating as soon as they are born. If conservative therapy fails to alleviate airway obstruction, surgical surgery may be considered. Patients with PRS require multidisciplinary approaches for treatment.
Abstract: Pierre Robin syndrome is a common craniofacial abnormality that causes glossoptosis and blockage of the upper airway. This renders it difficult to feed, which leads to severe malnutrition. This condition is also often marked by an absence of a soft palate. We mention a newborn with Pierre Robin syndrome with the absence of a soft palate and pneumonia complications, whose impending respiratory failure was treated successfully. To solve the complex problems that these babies and their families are facing, a multidisciplinary approach is needed.
Keywords: Pierre Robin syndrome; congenital defects; feeding problem; micrognathia; pediatrics; pneumonia; soft palate.
© 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Conflict of interest statement
The authors declare that they have no competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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