GALT deficiency/Galactosemia is a rare genetic disorder that affects how your body processes or metabolizes a sugar called galactose.Signs and symptoms include:An infant affected with galactosemia, appears normal at birth; however, within a few days or weeks, the infant may lose its appetite and start vomiting excessively.Yellowing of the skin, and mucous membranes, and whites of the eyes (jaun  Read More

Bacteria and animals cause lysosomal alpha-n-acetylgalactosaminidas. It is a glycoside hydrolase which is also known as nagalase. NAGA is an enzyme that is coded as a human gene that mutates. The mutations in the gene and the deficiency in alpha-N-acetylgalactosaminidase are caused due to Schindler disease. The activity of this enzyme converts type A blood to blood type O. Therefore, its name is A-zyme. Bacterial enzymes and A-zyme carry out r  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

Von-Gierke Disease, also known as Glycogen Storage Disease I is a rare genetic disorder characterized by the inability of the body to break down glycogen. Glycogen is the stored form of glucose present in the liver and muscles, which is usually broken down into simple glucose molecules to fuel the cells with energy.The condition occurs when the body lacks the absence of a specific enzyme, glucose-6-phosphatase that  Read More