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Pulmonary interstitial glycogenosis: An unrecognized etiology of persistent pulmonary hypertension of the newborn in congenital heart disease?

  • Author(s): Fineman, Jeffrey
  • Oishi, Peter
  • Radman, MR
  • Goldhoff, P
  • Jones, KD
  • Azakie, A
  • Datar, S
  • Adatia, I
  • Fineman, JR
  • et al.

Published Web Location

http://europepmc.org/articles/PMC3651824?pdf=render
No data is associated with this publication.
Abstract

Background: Pulmonary interstitial glycogenosis (PIG) arises from a developmental disorder of the pulmonary mesenchyme and presents clinically with reversible neonatal respiratory distress and/or persistent pulmonary hypertension of the newborn (PPHN). Obj

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