Cloacal dysgenesis sequence associated with esophageal atresia and tracheoesophageal fistula: A case report and review of literature
作者: Ramaswamy Rajendran Baz Rayan Ahmed Alchami Marwan Mukattash Ghazi <dc:subject xml:lang="en-US">pediatric surgery
刊名: Pediatric Urology Case Reports, 2019, Vol.6 (4)
来源数据库: Pediatric Urology Case Reports
DOI: 10.14534/j-pucr.2019452979
关键词: Cloacal dysgenesis sequenceAbsent perineal orificeAbsent external genitaliaCompressed chestUrorectal septum malformation sequence.
原始语种摘要: Absence of any orifice in perineum, presence of smooth perineum, and absence external genitalia are characteristic of cloacal dysgenesis sequence (CDS). Newborn of 40w gestational age, born to mother with oligohydramnios, had very low APGAR scores, and was put on ventilator. Child had dysmorphic facies, short neck, compressed chest, no urinary bladder swelling, absence of any perineal orifice, a raised fold of skin at the site of phallus and bilateral talipes calcaneovalgus. Esophageal atresia (EA) was diagnosed clinically and radiographically. Pulmonary hypoplasia, distal tracheoesophageal fistula (TOF), thin, flat and broad cervical vertebrae with spina bifida, partial sacral agenesis and cardiac anomalies were demonstrated by radiographs and echocardiography respectively. Child...
全文获取路径: 小儿泌尿外科病例报告 

  • atresia 闭锁
  • esophageal 食管的
  • sequence 次序
  • perineal 会阴的
  • talipes 畸形足
  • fistula 喙管
  • dysgenesis 发育不全
  • hypoplasia 发育不全
  • septum 隔壁
  • orifice 遮光板