Literature DB >> 29622709

More than meets the eye: infant presenting with hypoxic ischaemic encephalopathy.

Kuntal Sen1,2, Rajkumar Agarwal2,3.   

Abstract

We report a newborn infant who presented with poor Apgar scores and umbilical artery acidosis leading to the diagnosis of hypoxic ischaemic encephalopathy. During the course of the infant's hospitalisation, subsequent workup revealed an underlying genetic cause that masqueraded as hypoxic ischaemic encephalopathy. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  congenital disorders; neonatal and paediatric intensive care; neuro genetics

Mesh:

Substances:

Year:  2018        PMID: 29622709      PMCID: PMC5893988          DOI: 10.1136/bcr-2017-223614

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  3 in total

Review 1.  Congenital central hypoventilation syndrome: a neurocristopathy with disordered respiratory control and autonomic regulation.

Authors:  Casey M Rand; Michael S Carroll; Debra E Weese-Mayer
Journal:  Clin Chest Med       Date:  2014-07-26       Impact factor: 2.878

2.  An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.

Authors:  Debra E Weese-Mayer; Elizabeth M Berry-Kravis; Isabella Ceccherini; Thomas G Keens; Darius A Loghmanee; Ha Trang
Journal:  Am J Respir Crit Care Med       Date:  2010-03-15       Impact factor: 21.405

Review 3.  Congenital central hypoventilation syndrome and the PHOX2B gene: a model of respiratory and autonomic dysregulation.

Authors:  Pallavi P Patwari; Michael S Carroll; Casey M Rand; Rajesh Kumar; Ronald Harper; Debra E Weese-Mayer
Journal:  Respir Physiol Neurobiol       Date:  2010-06-30       Impact factor: 1.931

  3 in total

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