December 7, 2021

Glycogen storage disease type I (GSD-I) is an autosomal recessive disease in which the liver can’t metabolize stored glycogen into […]

Galactosemia is a rare hereditary disease in which galactose metabolism fails. This failure leads to galactose accumulation in the blood

Wilson’s disease is a genetic disorder that affects the liver, brain, and other organs by accumulating extra copper in their

Alpha-1 antitrypsin deficiency(AATD) is a rare genetic disease that causes lung, liver, and skin problems. The liver synthesizes alpha-1 antitrypsin