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Esophageal atresia and anal atresia in a newborn with heterotaxia combined with other congenital defects #MMPMID27625802
Smigiel R; Misiak B; Golebiowski W; Lebioda A; Dorobisz U; Zielinska M; Patkowski D
J Pediatr Genet 2012[Mar]; 1 (1): 55-8 PMID27625802show ga
Heterotaxia (HTX) is a heterogeneous group of laterality defects characterized by abnormal discordance of asymmetric thoracic and abdominal organs. Esophageal anomalies occur rarely in HTX cases although additional defects associated with esophageal atresia are common. We report on a rare case of a neonate with HTX and multiple congenital malformations as well as specific facial dysmorphism, corresponding only to a few cases described in literature. Clinical examination of the proband revealed esophageal atresia with distal tracheoesophageal fistula, anal atresia, abdominal situs inversus, dextrocardia with complex congenital heart defect and left lung agenesis. A complex genetic analysis revealed no genetic abnormalities. Despite extensive diagnostic procedures, the cause of the laterality sequence disruption remains unclear, indicating its multifactorial etiology.