2017年7月24日 · Argininemia is a rare inherited disorder caused by a deficiency of the enzyme arginase, which is essential for breaking down the amino acid arginine. This condition leads to …

2023年8月8日 · Arginase deficiency (argininemia) is an autosomal recessive metabolic disorder characterized by hyperammonemia secondary to arginine accumulation. The disorder is rare …

Argininemia is an autosomal recessive urea cycle disorder where a deficiency of the enzyme arginase causes a buildup of arginine and ammonia in the blood. Ammonia, which is formed …

Arginase deficiency is an inherited disorder that causes the amino acid arginine (a building block of proteins) and ammonia to accumulate gradually in the blood. Ammonia, which is formed …

Argininemia is a rare genetic disorder. People with argininemia have problems with an enzyme called arginase I as it is either missing, deficient, or damaged. The arginase I enzyme has an …

Argininemia is an inherited metabolic disease in which the body is unable to process arginine (a building block of protein). It belongs to a group of disorders known as urea cycle disorders. …

Argininemia is the only urea cycle defect in which cortical and pyramidal tract signs predominate. However, because of early recognition and initiation of treatment, more than 80% of reported …

2004年10月21日 · Arginase deficiency in untreated individuals is characterized by episodic hyperammonemia of variable degree that is infrequently severe enough to be life threatening …

What is Argininemia? Argininemia (ARG) is a condition that causes harmful amounts of arginine and ammonia to build up in the body. It is considered an amino acid condition because people …

Argininemia is a rare genetic disorder that affects the breakdown of amino acids in the body. It’s characterized by a deficiency of the enzyme arginase, which is responsible for converting …