Metabolic disorders such as argininosuccinic and glutaric aciduria, methylmalonic acidemia, homocystinuria or primary hyperoxaluria require specific diets to prevent the accumulation of substances ...

HEREDITARY orotic aciduria is a disorder of pyrimidine metabolism manifested by megaloblastic anemia, leukopenia, retarded growth and the urinary excretion of large quantities of orotic acid.1 , 2 ...

Reid Sutton, V, Pan, Y, Davis, EC, Craigen, WJ. A mouse model of argininosuccinic aciduria: biochemical characterization. Mol Genet Metab. 2003;78 (1):11–16.

Argininosuccinic Aciduria Market Outlook 2025-2035: The argininosuccinic aciduria market is demonstrating a promising trajectory, with a projected CAGR of 3.5% across the 7 major markets between 2025 ...

Scientists cured a genetic liver disease called Argininosuccinic aciduria (ACLD) using genetic scissors and stem cells, according to a report published by the University of Helsinki.

Researchers from the University of Helsinki and HUS Helsinki University Hospital have achieved a significant medical breakthrough by successfully correcting a genetic defect that causes a hereditary ...

Argininosuccinate lyase deficiency (ASLD), also known as argininosuccinic aciduria, is a disease that has been enriched in the Finnish genetic heritage. In this severe metabolic disease, the body does ...

Argininosuccinate lyase deficiency (ASLD), also known as argininosuccinic aciduria, is a disease that has been enriched in the Finnish genetic heritage.

Argininosuccinate lyase deficiency (ASLD), also known as argininosuccinic aciduria, is a disease that has been enriched in the Finnish genetic heritage. In this severe metabolic disease, the body ...

Argininosuccinate lyase deficiency (ASLD), also known as argininosuccinic aciduria, is a disease that has been enriched in the Finnish genetic heritage.