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Pulmonary Interstitial Glycogenosis: An Unrecognized Etiology of Persistent Pulmonary Hypertension of the Newborn in Congenital Heart Disease?

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). OBJECTIVE: We report two cases of PIG in patien...

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Detalhes bibliográficos
Main Authors: Radman, Monique R., Goldhoff, Patricia, Jones, Kirk D., Azakie, Anthony, Datar, Sanjeev, Adatia, Ian, Oishi, Peter E., Fineman, Jeffrey R.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3651824/
https://ncbi.nlm.nih.gov/pubmed/22614905
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00246-012-0371-z
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