A Novel Mutation in FOXF1 Gene Associated with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins, Intestinal Malrotation and Annular Pancreas

被引:6
作者
Miranda, Joana [1 ]
Rocha, Gustavo [1 ]
Soares, Paulo [1 ]
Morgado, Helder [2 ]
Baptista, Maria Joao [3 ]
Azevedo, Ines [4 ]
Fernandes, Susana [5 ]
Brandao, Otilia [6 ]
Sen, Partha [7 ]
Guimaraes, Hercilia [1 ]
机构
[1] Univ Porto, Ctr Hosp Sao Joao, Div Neonatol, Fac Med, P-4100 Oporto, Portugal
[2] Univ Porto, Ctr Hosp Sao Joao, Fac Med, Div Pediat Surg, P-4100 Oporto, Portugal
[3] Univ Porto, Ctr Hosp Sao Joao, Fac Med, Div Pediat Cardiol, P-4100 Oporto, Portugal
[4] Univ Porto, Ctr Hosp Sao Joao, Fac Med, Unit Pulmonol,Dept Pediat, P-4100 Oporto, Portugal
[5] Univ Porto, Ctr Hosp Sao Joao, Fac Med, Dept Genet, P-4200319 Oporto, Portugal
[6] Univ Porto, Ctr Hosp Sao Joao, Fac Med, Dept Anat Pathol, P-4200319 Oporto, Portugal
[7] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
关键词
Alveolar capillary dysplasia with misalignment of pulmonary veins; Persistent pulmonary hypertension of the newborn; Extracorporeal membrane oxygenation FOXF1; DUODENAL ATRESIA; LUNG; HAPLOINSUFFICIENCY; DILATATION; EXPRESSION;
D O I
10.1159/000346062
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Alveolar 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 (C) 2013 S. Karger AG, Basel
引用
收藏
页码:241 / 245
页数:5
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