Description
Screening examination to exclude inborn metabolic "errors" of the aminoacidopathy type (hereditary disorders of amino acid metabolism). Indicated for adults with severe metabolic disorders. Determined amino acids: alanine (ALA), arginine (ARG), citrulline (CIT), proline (PRO), glycine (GLY), methionine (MET), ornithine (ORN), phenylalanine (PHE), tyrosine (TYR), valine (VAL), leucine (LEU) + isoleucine (ILEU), aspartic acid (ASP), glutamic acid (GLU).
The study is intended only for persons older than 1 year.
Period of execution
Within 5 days. The specified time does not include the day of biomaterial collection
Biomaterial type