– Mitchell Magyar, teen with Argininosuccinic Aciduria (ASA)
Urea Cycle Disorders (UCDs) are a group of inherited conditions of protein metabolism that affect how the body removes ammonia. While these conditions vary, most people require a strict diet, medical formulas, and medications to manage long-term health. flok supports individuals and families living with:
Ornithine Transcarbamylase deficiency (OTC)
Citrullinemia (CIT)
Argininosuccinic Aciduria (ASA)
Arginase-1 Deficiency (ARG1-D)
N-Acetylglutamate Synthetase deficiency (NAGS)
Carbamoyl Phosphate Synthetase Deficiency (CPS)
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