Monique R. Radman

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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 patients with congenital heart disease (CHD) and evidence of(More)
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