Nutrition management of congenital glucose–galactose malabsorption
نویسندگان
چکیده
منابع مشابه
Lactose malabsorption and nutrition
© 2014 John Wiley & Sons, Ltd. Published 2014 by John Wiley & Sons, Ltd. The consumption of milk and dairy products varies considerably in different regions of the world. Indeed, according to the statistics of the Food and Agriculture Organization of the United Nations (FAO), in 2007 the consumption of milk and dairy products averaged 240 kg and 360 kg per capita in the UK and Sweden, respectiv...
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...
متن کاملCongenital lactose malabsorption.
Levin, B., Abraham, J. M., Burgess, E. A., and Waffis, P. G. (1970). Archives of Disease in Childhood, 45, 173. Congenital lactose malabsorption. A breastfed female infant is described who developed from the third day of life a severe watery diarrhoea, with weight loss. This ceased when lactose was omitted from the feeds and returned when it was resumed. Intolerance to this carbohydrate was con...
متن کاملCongenital glucose-galactose malabsorption in Arab children.
Eight children with chronic diarrhea from glucose-galactose malabsorption from eight different families are presented. Six children are Saudi Arabs and two are of the other Arab nationalities. The mean age of the children at the time of presentation was 10.6 months. They were first seen for chronic watery diarrhea, present since birth, and failure to thrive. Laboratory investigations, including...
متن کاملD28G mutation in congenital glucose-galactose malabsorption.
BACKGROUND Congenital glucose-galactose malabsorption is a rare autosomal recessive disorder of the intestinal transport of glucose and galactose, leading to watery diarrhea, dehydration, failure to thrive, and early death. METHODS In this study, we analyzed D28G mutation in 16 family members of a patient with typical presentation of congenital glucose-galactose malabsorption with polymerase ...
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ژورنال
عنوان ژورنال: Medicine
سال: 2019
ISSN: 0025-7974,1536-5964
DOI: 10.1097/md.0000000000016828