DGAT-1 deficiency is a rare genetic disease. If not treated, it can cause diarrhea, an inability to absorb nutrients, and poor growth. The condition usually starts soon after birth and is one of a group of disorders termed congenital diarrheas.
DGAT-1 (diacylglycerol-acyltransferase 1) is a protein that helps the body produce certain fats in the intestine called triglycerides. If the DGAT-1 protein malfunctions or is absent, symptoms can occur.