Congenital chloride diarrhea in dizygotic twins
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Seo, K.A. | - |
dc.contributor.author | Lee, Na Mi | - |
dc.contributor.author | Kim, Kwang Jun | - |
dc.contributor.author | Yun, Sin Weon | - |
dc.contributor.author | Chae, Soo Ahn | - |
dc.contributor.author | Lim, In Seok | - |
dc.contributor.author | Choi, E.S. | - |
dc.contributor.author | Yoo, B.H. | - |
dc.date.available | 2019-05-29T03:36:49Z | - |
dc.date.issued | 2013-09 | - |
dc.identifier.issn | 2234-8646 | - |
dc.identifier.issn | 2234-8840 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/19823 | - |
dc.description.abstract | Congenital chloride diarrhea (CLD) is a rare inherited autosomal recessive disorder. Mutations of the solute carrier family 26 member 3 gene cause profuse, chloride ion rich diarrhea, which results in hypochloremia, hyponatremia and metabolic alkalosis with dehydration. If a fetal ultrasound shows bowel dilatation suggestive of bowel obstruction, or if a neonate shows persistent diarrhea and metabolic alkalosis, CLD should be considered in the differential diagnosis. The severity of CLD varies, but early detection and early therapy can prevent complications including growth failure. We report a case of dizygotic twins affected by CLD who had been born to non-consanguineous parents. Both of them showed growth failure, but one of the twins experienced worse clinical course. He showed developmental delay, along with dehydration and severe electrolyte imbalance. He was diagnosed with CLD first at 6-month age, and then the other one was also diagnosed with CLD. © 2014 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition. | - |
dc.format.extent | 5 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Korean Society of Pediartic Gastroenterology, Hepatology and Nutrition | - |
dc.title | Congenital chloride diarrhea in dizygotic twins | - |
dc.type | Article | - |
dc.identifier.doi | 10.5223/pghn.2013.16.3.195 | - |
dc.identifier.bibliographicCitation | Pediatric Gastroenterology, Hepatology and Nutrition, v.16, no.3, pp 195 - 199 | - |
dc.identifier.kciid | ART001811663 | - |
dc.description.isOpenAccess | Y | - |
dc.identifier.scopusid | 2-s2.0-84951930237 | - |
dc.citation.endPage | 199 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 195 | - |
dc.citation.title | Pediatric Gastroenterology, Hepatology and Nutrition | - |
dc.citation.volume | 16 | - |
dc.type.docType | Article | - |
dc.publisher.location | 대한민국 | - |
dc.subject.keywordAuthor | Alkalosis | - |
dc.subject.keywordAuthor | Congenital chloride diarrhea | - |
dc.subject.keywordAuthor | Dizygotic twins | - |
dc.subject.keywordAuthor | Hyponatremia | - |
dc.subject.keywordAuthor | Polyhydramnios | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
84, Heukseok-ro, Dongjak-gu, Seoul, Republic of Korea (06974)02-820-6194
COPYRIGHT 2019 Chung-Ang University All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.