Progress of the congenital glucose-galactose malabsorption / 国际儿科学杂志

ABSTRACT

Congenital glucose-galactose malabsorption(CGGM),also known as congenital glucose-ga-lactose intolerance syndrome,is a rare autosomal recessive hereditary disease.Domestic research about CGGM is rare and there was no discovery of the cases for this disease.This review summarizes the mechanism,clinical characteristics,diagnosis and treatment of CGGM.