Clinical Characteristics and Treatment of Currarino Syndrome: A Single Institutional Experience
Open Access
- 1 January 2020
- journal article
- research article
- Published by XMLink in Advances in Pediatric Surgery
- Vol. 26 (2) , 46-53
Abstract
Kim HJ, et al. Adv Pediatr Surg. 2020 Dec;26(2):46-53. https://doi.org/10.13029/aps.2020.26.2.46Keywords
This publication has 17 references indexed in Scilit:
- Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype? A multicentre studyJournal of Pediatric Surgery, 2017
- The Currarino triad: What pediatric surgeons need to knowJournal of Pediatric Surgery, 2017
- Multidisciplinary surgical treatment of presacral meningocele and teratoma in an adult with Currarino triadSurgical Neurology International, 2017
- Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino casesEuropean Journal of Medical Genetics, 2013
- Long-term functional outcomes in children with Currarino syndromePediatric Surgery International, 2010
- Variable presentations of Currarino syndrome in three members of the same familyActa Neurochirurgica, 2009
- The Currarino triad: the variable expressionJournal of Pediatric Surgery, 2005
- Currarino syndrome: Proposal of a diagnostic and therapeutic protocolJournal of Pediatric Surgery, 2004
- The Currarino triad: complex of anorectal malformation, sacral bony abnormality, and presacral massPediatric Radiology, 1984
- Triad of anorectal, sacral, and presacral anomaliesAmerican Journal of Roentgenology, 1981