Congenital glucose-galactose malabsorption: A case report about cause and consequence, not exactly in this order
Congenital glucose-galactose malabsorption (CGGM) is a rare metabolic disorder caused by a deficient intestinal sodium-dependent glucose cotransporter (SGLT1) protein. Its failure leads to a lack of absorption of galactose, glucose, and sodium, which remains inside the intestinal lumen. The conseque...
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Main Authors: | , , , , , |
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Format: | Book |
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Elsevier,
2024-09-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |