Case report: Diagnosis and treatment of DGAT1 deficiency-induced congenital diarrhea in two cases and literature review
IntroductionCongenital diarrhea is a rare inherited intestinal disease characterized by persistent and severe diarrhea and malabsorption in the first few weeks after birth, which can be life-threatening. Some congenital diarrheal diseases are associated with mutations in the diacylglycerol acyltrans...
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