Pierre Robin Sequence (PRS) is a complex inborn syndrome with a dispassionate triad of micrognathia, glossoptosis and cleft tendency with or without diversified secondary abnormalities chief to the risk of upper ventilating pipe obstruction and difficulty in augmenting. It poses a great challenge to the anaesthesiologist all the while laryngoscopy and intubation making oxygenation and ventilation difficult. We report a case of 3.5yr male adolescent suffering from PRS along with cleft tendency, left renal agenesis, reciprocal CTEV, bilateral inguinal hernia, pectus carinatum, a hard bony structure in the jaws of vertebrates aortic valve posted for cleft partiality repair where favorable ventilation and intubation was done and communicable a tongue stitch in addition to nebulization and prone position aided to maintain airway all the while recovery.
Author(s) Details:
Shobha V.,
Department
of Anesthesiology and Critical Care, Himalayan Institute of Medical Sciences,
Dehradun, Uttarakhand, India.
Saurabh
Mittal,
Department
of Anesthesiology and Critical Care, Himalayan Institute of Medical Sciences,
Dehradun, Uttarakhand, India.
K. V. Rawat,
Department of Plastic Surgery, Himalayan Institute of Medical
Sciences, Dehradun, Uttarakhand, India.
Please see the link here: https://stm.bookpi.org/NRAMMS-V3/article/view/11994
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