• Joana Miranda, Gustavo Rocha, Paulo Soares, Hélder Morgado, Maria João Baptista, Inês Azevedo, Susana Fernandes, Otília Brandão, Partha Sen, and Hercília Guimarães.
• Division of Neonatology, Centro Hospitalar de São João, Faculty of Medicine of Porto University, Porto, Portugal. joanam@gmail.com
• Neonatology. 2013 Jan 1; 103 (4): 241-5.

AbstractAlveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is a rare, fatal, neonatal developmental lung disorder, which usually presents as persistent pulmonary hypertension unresponsive to treatment. The authors report the case of a neonate with persistent pulmonary hypertension, associated with duodenal stenosis secondary to annular pancreas and intestinal malrotation. Support treatment, inhaled nitric oxide, oral sildenafil and nebulized iloprost were used with no clinical improvement. The neonate presented an overwhelming course, with hypoxemia refractory to treatment. At autopsy lung histology showed the characteristic features of ACD/MPV. DNA sequence analysis revealed a heterozygous nonsense mutation c.539C>A;p.S180X, in the first exon of FOXF1. FOXF1 has been identified as one of the genes responsible for ACD/MPV associated with multiple congenital malformations. This clinical case is the first report of a heterozygous nonsense mutation c.539C>A;p.S180X in the first exon of FOXF1, in a patient with ACD/MPV associated with annular pancreas and intestinal malrotation.Copyright © 2013 S. Karger AG, Basel.

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