Dubin-Jhonson syndrome is a rare genetic liver disorder that is inherited by the autosomal recessive pattern ( inherit one mutated gene from each parent ). It is characterized by the breakdown of red blood cells into the yellowish pigment in the blood that results in bilirubin buildup. Moreover, this buildup is released into the bile, a digestive juice secreted by the liver. Moreover, this pigment gives stool a deep yellowish  Read More

Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a disorder in which the body is unable to convert specific fats to energy, particularly when fasting (fasting).Low blood sugar (hypoglycemia), tiredness (lethargy), and muscle weakness are major symptoms of VLCAD deficiency in infancy and early childhood.Individuals who are affected are also at risk of major consequences, including liver problems  Read More