Glucose-Galactose Malabsorption

Watchlist

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Retrieved

2021-01-23

Source

Orphanet

Trials

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Genes

SLC5A1, SLC5A2, ABO, SERPINA1, CXCL13, TP53, SLC2A2, PTEN, PROX1, LBP, C5AR1, LAMC2, HHEX, GH1, GFAP, CSF2, CR1, CD14, TRPV6

Drugs

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Glucose-galactose malabsorption (GGM) is a very rare, potentially lethal, genetic metabolic disease characterized by impaired glucose-galactose absorption resulting in severe watery diarrhea and dehydration with onset inthe neonatal period.