文章基本信息

标题：A Case Report of Glucose-Galactose Malabsorption in Iranian Child
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作者：Pantea Tajik ; Amir Hossein Goudarzian ; Zeinab Pourzahabi 等
期刊名称：International Journal of Pediatrics
印刷版ISSN：2345-5047
电子版ISSN：2345-5055
出版年度：2019
卷号：7
期号：5
页码：9399-9403
DOI：10.22038/ijp.2019.35793.3124
出版社：Mashhad University of Medical Sciences
摘要：Introduction
Glucose-Galactose Malabsorption (GGM) is an autosomal recessive and rare disorder of intestinal transport of glucose and sodium-glucose cotransporter type (SGLT1).
Case Report
Our patient is a 32-day-old boy who was examined for severe diarrhea and acidosis and was treated with GGMdiagnosis. A number of laboratory tests were performed on this patient as well as positive test for reduced substance of stool and positive hydrogen breath test. On the other hand, the improvement of diarrhea with fasting and the initiation of a glucose and galactose free formula (fructose-based formula [galactomin B-19]) was instructed. He was treated and followed with diagnosis of GGM.
Conclusion
In summary, careful clinical observation, laboratory tests, and the character of the external cues may provide indications of GGM.
关键词：case report; Child; Diarrhea; Glucose-Galactose Malabsorption