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  • Recurrent apnoea and respiratory failure in an infant: congenital central hypoventilation syndrome with a novel PHOX2B gene variant

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Case report
Recurrent apnoea and respiratory failure in an infant: congenital central hypoventilation syndrome with a novel PHOX2B gene variant

Authors

  1. Correspondence to Dr Ajay S Kasi; ajay.kasi{at}emory.edu
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Citation

Anand N, Leu RM, Simon D, et al
Recurrent apnoea and respiratory failure in an infant: congenital central hypoventilation syndrome with a novel PHOX2B gene variant
BMJ Case Reports CP 2021;14:e239633.

Publication history

  • Accepted March 5, 2021
  • First published March 19, 2021.
Online issue publication 
January 24, 2024

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© BMJ Publishing Group Limited 2021. No commercial re-use. See rights and permissions. Published by BMJ.