Glucose-galactose malabsorption: a case report

Glucose-Galactose Malabsorption (GGM) is one of the rare autosomal recessive disorders of intestinal transport of glucose and galactose/Na+cotransport system (SGLT1) that leads to osmotic watery diarrhea, dehydration, failure to thrive, or early death. It is caused by mutations in the gene coding fo...

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Asıl Yazarlar: Farid Imanzade (Yazar), Aliakbar Sayarri (Yazar), Abdolhamid Sharifian (Yazar), Pantea Tajik (Yazar)
Materyal Türü: Kitap
Baskı/Yayın Bilgisi: Islamic Azad University, 2014-12-01T00:00:00Z.
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