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Case Report

Familial Isolated Anorectal Malformation: A Case Report

Journal of the Korean Association of Pediatric Surgeons 2017;23(1):12-14.
Published online: June 26, 2017

Department of Surgery, Kyungpook National University School of Medicine, Daegu, Korea.

Correspondence: Jinyoung Park, Department of Surgery, Kyungpook National University Hospital, 130 Dongdeok-ro, Jung-gu, Daegu 41944, Korea. Tel: +82-53-420-5612, Fax: +82-53-421-0510, kpnugs@knu.ac.kr
• Received: November 22, 2016   • Revised: May 6, 2017   • Accepted: May 10, 2017

Copyright © 2017 Korean Association of Pediatric Surgeons

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • There have been a few reports of familial anorectal malformations extending over more than one generation. We experienced a case of a family with 3 members spanning 2 generations affected with isolated low type anorectal malformations. They had same low type of anorectal malformations. In all 3 patients, a perianal anoplasty was performed.

No potential conflict of interest relevant to this article was reported.

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Fig. 1

Perineal subepithelial midline raphe fistula that meconium comes out.

jkaps-23-12-g001.jpg

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Familial Isolated Anorectal Malformation: A Case Report
J Korean Assoc Pediatr Surg. 2017;23(1):12-14.   Published online June 26, 2017
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Familial Isolated Anorectal Malformation: A Case Report
J Korean Assoc Pediatr Surg. 2017;23(1):12-14.   Published online June 26, 2017
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Familial Isolated Anorectal Malformation: A Case Report
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Fig. 1 Perineal subepithelial midline raphe fistula that meconium comes out.
Familial Isolated Anorectal Malformation: A Case Report