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The Currarino Triad.

作者信息

Vinod M S, Chandra Shaw Subhash, Devgan Amit, Mukherjee Sweta

机构信息

Classified Specialist (Surgery) and Paediatric Surgeon, Command Hospital (Eastern Command), Kolkata, India.

Associate Professor (Paediatrics), Armed Forces Medical College, Pune 411040, India.

出版信息

Med J Armed Forces India. 2018 Oct;74(4):374-376. doi: 10.1016/j.mjafi.2017.07.006. Epub 2017 Aug 18.

DOI:10.1016/j.mjafi.2017.07.006
PMID:30449925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6224645/
Abstract
摘要

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The Currarino triad: the variable expression.库拉里诺三联征:可变表现。
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本文引用的文献

1
The Currarino triad: What pediatric surgeons need to know.库拉里诺三联征:小儿外科医生需要了解的内容。
J Pediatr Surg. 2017 Aug;52(8):1260-1268. doi: 10.1016/j.jpedsurg.2016.12.010. Epub 2016 Dec 27.
2
Currarino Syndrome and the Effect of a Large Anterior Sacral Meningocele on Distal Colostogram in an Anorectal Malformation.库拉里诺综合征及巨大骶前脊膜膨出对肛门直肠畸形患者远端结肠造影的影响。
J Radiol Case Rep. 2016 Jun 30;10(6):16-21. doi: 10.3941/jrcr.v10i6.2068. eCollection 2016 Jun.
3
A Very Rare Cause of Anal Atresia: Currarino Syndrome.肛门闭锁的一种极为罕见的病因:库拉里诺综合征。
J Clin Med Res. 2016 May;8(5):420-3. doi: 10.14740/jocmr2505w. Epub 2016 Mar 20.
4
A missed case of Currarino syndrome.
Clin Pediatr (Phila). 2010 Feb;49(2):183-5. doi: 10.1177/0009922809350219.
5
Currarino syndrome: proposal of a diagnostic and therapeutic protocol.库拉里诺综合征:诊断与治疗方案建议
J Pediatr Surg. 2004 Sep;39(9):1305-11. doi: 10.1016/j.jpedsurg.2004.05.003.
6
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.一种同源框基因HLXB9是显性遗传骶骨发育不全的主要位点。
Nat Genet. 1998 Dec;20(4):358-61. doi: 10.1038/3828.
7
A novel embryogenetic mechanism for Currarino's triad: inadequate dorsoventral separation of the caudal eminence from hindgut endoderm.
Pediatr Neurosurg. 1998 May;28(5):223-9. doi: 10.1159/000028655.
8
Currarino triad: anorectal malformation, sacral bony abnormality, and presacral mass--a review of 11 cases.库里亚里诺三联征:肛门直肠畸形、骶骨骨质异常和骶前肿块——11例病例回顾
J Pediatr Surg. 1997 Jan;32(1):58-61. doi: 10.1016/s0022-3468(97)90094-4.
9
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36.
Nat Genet. 1995 Sep;11(1):93-5. doi: 10.1038/ng0995-93.
10
Triad of anorectal, sacral, and presacral anomalies.
AJR Am J Roentgenol. 1981 Aug;137(2):395-8. doi: 10.2214/ajr.137.2.395.