You are here

  • Home
  • Archive
  • Volume 96, Issue 6
  • Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis

Article info

Article menu
Download PDFPDF
Short reports
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis

Authors

  1. Correspondence to Professor Andreas Holzinger, Dr von Hauner Children's Hospital, Ludwig-Maximilian University Munich, Lindwurmstrasse 4, Munich, 80337, Germany; andreas.holzinger{at}med.uni-muenchen.de
View Full Text

Citation

Kleinlein B, Griese M, Liebisch G, et al
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis
Archives of Disease in Childhood - Fetal and Neonatal Edition 2011;96:F453-F456.

Publication history

  • Accepted April 18, 2010
  • First published June 28, 2010.
Online issue publication 
October 26, 2017

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Copyright information

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions