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Pulmonary interstitial glycogenosis: An unrecognized etiology of persistent pulmonary hypertension of the newborn in congenital heart disease?
Published Web Location
http://europepmc.org/articles/PMC3651824?pdf=renderNo 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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