Glycogen storage diseases are a group of disorders in which stored glycogen cannot be metabolized into glucose to supply energy and to maintain steady blood glucose levels for the body.Glycogen storage disease I (GSDI) is inherited as an autosomal recessive genetic disorder.The disorder is characterized by the accumulation of excess glycogen and fat in the liver and kidneys, resulting in an enlarged liver  Read More

Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a condition that restricts the body from converting specific fats to energy, especially during periods of fasting.The symptoms of LCAD deficiency appear during infancy or early childhood.It involves hypoglycemia (low blood sugar), lethargy (lack of energy) and muscle weakness.The individuals who are affected by this disorder are also hig  Read More