A case of Pierre Robin syndrome in a child with no soft palate and complications from pneumonia in Bangladesh

Author:

Amin Mohammad Ashraful12ORCID,Shawon Taraque Ahamed3,Shaon Naushad Khan4,Nahin Sabrina5,Fardous Jannatul6,Hawlader Mohammad Delwer Hossain1ORCID

Affiliation:

1. Department of Public Health North South University Dhaka Bangladesh

2. Public Health Professional Development Society (PPDS) Dhaka Bangladesh

3. Department of Pediatric, Maternal and Child Health Training Institute (MCHTI) Ministry of Health and Family Welfare Dhaka Bangladesh

4. Department of Anesthesia Bangabandhu Sheikh Mujib Medical University Hospital Dhaka Bangladesh

5. Department of Physiology Green Life Medical College Hospital Dhaka Bangladesh

6. Department of Paediatric Nephrology National Institute of Kidney Diseases & Urology (NIKDU) Dhaka Bangladesh

Abstract

Key Clinical MessageChildren 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.AbstractPierre 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.

Publisher

Wiley

Subject

General Medicine

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