Congental Glucose- Galactose Malabsorption a Rare Cause of Diarrhea in Infancy Period: Report of Two Cases
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A Case Report of Glucose-Galactose Malabsorption in Iranian Child
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 r...
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Congenital glucose-galactose malabsorption (CGGM) is a rare cause of intractable infantile diarrhea, with only a few hundred cases recognized worldwide. This life-threatening disorder must be considered in the differential diagnosis of an infant who presents with diarrhea and dehydration that fails to respond to standard therapy. The clinical and diagnostic course of an infant with recurrent ep...
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متن کاملCongenital glucose galactose malabsorption.
Introduction Congenital glucose galactose malabsorption (CGGM) is a rare autosomal recessive disorder, which presents as a protracted diarrhoea in early neonatal life. It is due to a defect in sodium coupled transport of glucose and galac tose in the enterocyte (1). Diarrhoea in CGGM is osmotic, caused by accumulation of unabsorbed glucose and ga lactose in the intestine (2), which results in...
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عنوان ژورنال
دوره 2 شماره 2
صفحات 119- 123
تاریخ انتشار 2003-06
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