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 …

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 …

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 …

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 that affects how the body breaks down the amino acid arginine. This condition is caused by a deficiency in the enzyme arginase, which is essential …

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 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 …

A rare autosomal recessive amino acid metabolism disorder characterized clinically by variable degrees of hyperammonemia, developing from about 3 years of age, and leading to …

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 …

Arginase is the enzyme involved in the last step of the urea cycle. It catalyzes the conversion of arginine to urea and ornithine. The latter reenters the mitochondrion to continue the cycle. …