Glutathione Synthetase Deficiency is a rare genetic disorder that affects the body's ability to produce an important antioxidant called glutathione. It is not contagious and cannot be transmitted from person to person. This condition is inherited in an autosomal recessive manner, meaning both parents must carry a mutated gene for their child to be affected. Glutathione Synthetase Deficiency can lead to various symptoms and health complications, and it requires medical management and support.
Glutathione Synthetase Deficiency is a rare genetic disorder that affects the body's ability to produce an important antioxidant called glutathione. This deficiency can lead to a variety of symptoms, including anemia, neurological problems, and an increased susceptibility to oxidative stress.
It is important to note that Glutathione Synthetase Deficiency is not contagious. It is an inherited condition caused by mutations in the GSS gene, which is responsible for producing the enzyme glutathione synthetase. These mutations are passed down from parents to their children and can result in a deficiency of glutathione synthetase.
The condition is inherited in an autosomal recessive manner, meaning that both parents must carry a copy of the mutated gene for their child to be affected. If both parents are carriers, there is a 25% chance with each pregnancy that their child will inherit two copies of the mutated gene and develop Glutathione Synthetase Deficiency.
While Glutathione Synthetase Deficiency is not contagious, it is important for individuals with the condition to receive appropriate medical care and management. Treatment may involve supplementation with glutathione or other antioxidants to help alleviate symptoms and reduce oxidative stress.