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International Journal of Pediatrics، جلد ۷، شماره ۵، صفحات ۹۳۹۹-۹۴۰۳
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
A Case Report of Glucose-Galactose Malabsorption in Iranian Child |
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| چکیده انگلیسی مقاله |
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-basedformula [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. |
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| کلیدواژه‌های انگلیسی مقاله |
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| نویسندگان مقاله |
| Pantea Tajik
Assistant Professor of Pediatric Gastroenterohepatology, Amiralmomenin Hospital, Semnan, Iran.
| Amir Hossein Goudarzian
MSc. Student of Nursing, Student Research Committee, Mazandaran University of Medical Sciences, Sari, Iran.
| Zeinab Pourzahabi
Pediatric Resident, Amiralmomenin Hospital, Semnan, Iran.
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| نشانی اینترنتی |
http://ijp.mums.ac.ir/article_12259.html |
| فایل مقاله |
اشکال در دسترسی به فایل - ./files/site1/rds_journals/317/article-317-1304333.pdf |
| کد مقاله (doi) |
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| زبان مقاله منتشر شده |
en |
| موضوعات مقاله منتشر شده |
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| نوع مقاله منتشر شده |
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