Aim Congenital glucose–galactose malabsorption (CGGM) is a rare disease characterised
by severe diarrhoea, dehydration and weight loss. To better understand CGGM, we …

Hypoaldosteronism is associated with either insufficient aldosterone production or lack of
responsiveness to aldosterone and can be isolated or in the context of primary adrenal …

Congenital glucose-galactose malabsorption (CGGM) is a rare metabolic disorder caused
by a deficient intestinal sodium-dependent glucose cotransporter (SGLT1) protein. Its failure …

Congenital glucose-galactose malabsorption is a rare cause of life-threatening diet-induced
diarrhea in infants. Mutations in the SLC5A1 gene, which encodes for the sodium …

Intractable watery diarrhea presenting in the neonatal period is a relatively uncommon
condition. Congenital disorders of malabsorption are among the major causes of prolonged …