A case of split notochord syndrome with congenital ileal atresia, the total absence of a colon, and a dorsal enteric cyst communicating to the retroperitoneal isolated ceca with a vesical fistula-Reference-Cited by-同舟云学术

A case of split notochord syndrome with congenital ileal atresia, the total absence of a colon, and a dorsal enteric cyst communicating to the retroperitoneal isolated ceca with a vesical fistula

Published:2008-07-30 Issue:9 Volume:24 Page:1073-1077
ISSN:0179-0358
Container-title:Pediatric Surgery International
language:en
Short-container-title:Pediatr Surg Int

Author:

Asagiri Kimio,Yagi Minoru,Tanaka Yoshiaki,Akaiwa Masao,Asakawa Takahiro,Kaida Akiko,Kobayashi Hidefumi,Tanaka Hiroaki

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Surgery,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00383-008-2206-9.pdf

Reference21 articles.

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2. Saunders RL (1943) Combined anterior and posterior spina bifida in a living neonatal female. Anat Rec 87:255–278

3. Rosselet PJ (1995) A rare case of rachischisis with multiple malformations. Am J Roentgenol Radium Ther Nucl Med 73:235–240

4. Bentley JFR, Smith JR (1960) Developmental posterior enteric remnants and spinal malformations. Arch Dis Child 35:76–86

5. Faris JC, Crowe JE (1975) The split notochord syndrome. J Pediatr Surg 4:467–472

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