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- W2044162802 abstract "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 severe malnu trition (3). When glucose and galactose are eliminated from the diet, infants with CGGM thrive and dietary interven tion after early diagnosis will result in normal growth and development." @default.
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- W2044162802 date "2014-02-04" @default.
- W2044162802 modified "2023-09-26" @default.
- W2044162802 title "Congenital glucose galactose malabsorption" @default.
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- W2044162802 doi "https://doi.org/10.4038/cmj.v46i1.6532" @default.
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