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- W2010015552 abstract "A newborn with persistent pulmonary hypertension (PH) unresponsive to conventional therapies was found to be homozygous for a mutation in the gene encoding adenosine triphosphate binding cassette protein, member A3 (ABCA3). Most causes of PH respond to lung recruitment, inhaled nitric oxide, and hemodynamic support. When PH is prolonged and does not respond to standard therapies, genetic causes of surfactant abnormalities should be considered in the differential diagnosis." @default.
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- W2010015552 date "2007-09-01" @default.
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- W2010015552 title "ABCA3 Deficiency Presenting as Persistent Pulmonary Hypertension of the Newborn" @default.
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- W2010015552 doi "https://doi.org/10.1016/j.jpeds.2007.05.054" @default.
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