Single-stage surgical correction of anorectal malformation associated with rectourinary fistula in male neonates [0.03%]
合并有直肠尿道瘘的男新生儿肛门闭锁的一期手术治疗
Ernesto Leva,Francesco Macchini,Rossella Arnoldi et al.
Ernesto Leva et al.
Introduction: The treatment of children affected by anorectal malformations (ARM) is characterized by some unsolved problems. The three-stage surgical correction has been known to be most effective in preventing complicat...
Yogesh Kumar Sarin
Yogesh Kumar Sarin
Naeem Khan
Naeem Khan
Lubna Ijaz,Bilal Mirza
Lubna Ijaz
Case Reports
Journal of neonatal surgery. 2012 Oct 1;1(4):61. DOI: 2012
Gastroschisis [0.03%]
腹裂
Vivek Gharpure
Vivek Gharpure
Anorectal malformation associated with small and large bowel atresias: a rare association [0.03%]
与小肠和大肠闭锁相关的肛门直肠畸形：一种罕见的并发症
Sujay Maitra,Ruchirendu Sarkar
Sujay Maitra
Yavuz Yilmaz,Gulsum Kadioglu,Hulya Ozkan-Ulu et al.
Yavuz Yilmaz et al.
Large gastric perforation in carmi syndrome: a morbid complication in a rare association [0.03%]
卡米综合征的巨大胃穿孔：一种罕见病的严重并发症
M Joshi,L Krishnan,S Kuruvila
M Joshi
The association between epidermolysis bullosa (EB) and congenital pyloric atresia (CPA) named Carmi Syndrome is rare. We report unusual and morbid complication of gastric perforation resulting in peritonitis in a preterm neonate born with C...
Case Reports
Journal of neonatal surgery. 2012 Oct 1;1(4):57. DOI: 2012
Sundeep Kisku,Sudipta Sen,Reju Joseph Thomas et al.
Sundeep Kisku et al.
Metabolic acidosis is often encountered in a sick neonate and intestinal duplication with heterotopic gastric mucosa is a well-established condition. We present a previously unreported relationship between neonatal metabolic acidosis, resul...
Case Reports
Journal of neonatal surgery. 2012 Oct 1;1(4):56. DOI: 2012
Diagnostic difficulties in a case of persistent cloaca with hydrocolpos [0.03%]
持续性肛门直肠畸形合并水囊阴道一例中的诊断困难
Zeki Sahinoglu,Aysenur Cerrah Celayir,Mehmet Resit Asoglu et al.
Zeki Sahinoglu et al.
Pelvic midline cystic mass associated with renal malformation represents typical imaging features of a cloacal anomaly. We report a case of persistent cloaca that was diagnosed antenatally with fetal ultrasonography and MRI. ...
Case Reports
Journal of neonatal surgery. 2012 Oct 1;1(4):55. DOI: 2012