مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

A Case Report of Glucose-Galactose Malabsorption in Iranian Child

Pages

  9399-9403

Abstract

 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 GGM diagnosis. 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.

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    Cite

    APA: Copy

    TAJIK, PANTEA, Goudarzian, Amir Hossein, & Pourzahabi, Zeinab. (2019). A Case Report of Glucose-Galactose Malabsorption in Iranian Child. INTERNATIONAL JOURNAL OF PEDIATRICS, 7(5 (65)), 9399-9403. SID. https://sid.ir/paper/337689/en

    Vancouver: Copy

    TAJIK PANTEA, Goudarzian Amir Hossein, Pourzahabi Zeinab. A Case Report of Glucose-Galactose Malabsorption in Iranian Child. INTERNATIONAL JOURNAL OF PEDIATRICS[Internet]. 2019;7(5 (65)):9399-9403. Available from: https://sid.ir/paper/337689/en

    IEEE: Copy

    PANTEA TAJIK, Amir Hossein Goudarzian, and Zeinab Pourzahabi, “A Case Report of Glucose-Galactose Malabsorption in Iranian Child,” INTERNATIONAL JOURNAL OF PEDIATRICS, vol. 7, no. 5 (65), pp. 9399–9403, 2019, [Online]. Available: https://sid.ir/paper/337689/en

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