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Congenital Glucose-Galactose Malabsorption: A Rare Cause of Intractable Diarrhea in Infancy.

作者信息

Rath Ashwinee, Sethi Samir, Pattanaik Biswajit

机构信息

Department of Pediatrics, MKCG Medical College, Berhampur, Odisha, India.

出版信息

Indian Pediatr. 2025 Sep 8. doi: 10.1007/s13312-025-00187-2.

DOI:10.1007/s13312-025-00187-2
PMID:40920309
Abstract
摘要

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Congenital Glucose-Galactose Malabsorption: A Rare Cause of Intractable Diarrhea in Infancy.先天性葡萄糖-半乳糖吸收不良:婴儿期顽固性腹泻的罕见病因。
Indian Pediatr. 2025 Sep 8. doi: 10.1007/s13312-025-00187-2.
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本文引用的文献

1
Congenital Chloride Diarrhea in Infancy: Unveiling a Rare Clinical Case.婴儿期先天性氯腹泻:揭示一例罕见临床病例。
Indian Pediatr. 2025 Apr;62(4):293-294. doi: 10.1007/s13312-025-00041-5. Epub 2025 Apr 3.
2
Enteroendocrine Dysfunction in Two Saudi Sisters.两名沙特姐妹的肠内分泌功能障碍
Case Rep Gastroenterol. 2021 Mar 4;15(1):290-295. doi: 10.1159/000511761. eCollection 2021 Jan-Apr.
3
Congenital glucose-galactose malabsorption: A case report with a novel mutation.先天性葡萄糖-半乳糖吸收不良:一例伴有新突变的病例报告。
Clin Case Rep. 2018 Nov 11;7(1):51-53. doi: 10.1002/ccr3.1913. eCollection 2019 Jan.
4
Two Cases of Mistaken Polyuria and Nephrocalcinosis in Infants with Glucose-Galactose Malabsorption: A Possible Role of 1,25(OH)2D3
.葡萄糖-半乳糖吸收不良婴儿中两例多尿和肾钙质沉着误诊病例:1,25(OH)2D3的可能作用
Horm Res Paediatr. 2017;87(4):277-282. doi: 10.1159/000454951. Epub 2017 Feb 2.
5
Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene.一名土耳其新生儿的先天性葡萄糖-半乳糖吸收不良:钠/葡萄糖协同转运蛋白基因的新突变
Dig Dis Sci. 2017 Jan;62(1):280-281. doi: 10.1007/s10620-016-4348-2. Epub 2016 Oct 25.
6
Five Arab children with glucose-galactose malabsorption.五名患有葡萄糖-半乳糖吸收不良的阿拉伯儿童。
Paediatr Int Child Health. 2013 May;33(2):108-10. doi: 10.1179/2046905513Y.0000000055.
7
Identification of EpCAM as the gene for congenital tufting enteropathy.鉴定EpCAM为先天性簇状肠病的致病基因。
Gastroenterology. 2008 Aug;135(2):429-37. doi: 10.1053/j.gastro.2008.05.036. Epub 2008 May 15.
8
Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.葡萄糖-半乳糖吸收不良中的肾钙质沉着症:一名患有SGLT1新突变的幼儿的肾钙质沉着症和近端肾小管功能障碍
Eur J Pediatr. 2008 Dec;167(12):1395-8. doi: 10.1007/s00431-008-0681-6. Epub 2008 Feb 21.
9
Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis.葡萄糖-半乳糖吸收不良中的肾钙质沉着症,与肾小管酸中毒的关联。
Pediatr Nephrol. 2005 Sep;20(9):1336-9. doi: 10.1007/s00467-005-1885-x. Epub 2005 Jul 12.