Description
Quantitative study to detect functional metabolic changes (48 parameters) to assess amino acid metabolism, rule out inborn errors of metabolism such as aminoacidopathies, and detect functional imbalance.
Recommended for systemic nosological conditions in children older than 1 year and adults with severe metabolic disorders, and amino acid reabsorption disorders. Allows detecting amino acid metabolism disorders.
Composition of the study
1. 1-Methylhistidine (1-Methylhistidine)
2. 3-Methylhistidine (3-Methylhistidine)
3. N-acetyltyrosine
4. N-acetylphenylalanine (N-acetyl-L-phenylalanine)
5. N-acetylcysteine
6. N-acetylaspartate (NAA)
7. Alpha-aminoadipic acid (a-aminoadipic acid) (AAA)
8. Alpha-aminobutyric acid (a-aminobutyric acid)
9. Beta-alanine (b-alanine) (Beta-Alanine)
10. Beta-aminoisobutyric acid (b-aminoisobutyric acid)
11. Gamma-aminobutyric acid (y-aminobutyric acid)
12. Alanine (Alanine)
13. Allo-isoleucine (Allolle)
14. Anserine (Anserine)
15. Arginine (Arginine)
16. Argininosuccinic acid
17. Asparagine (ASN)
18. Aspartic Acid (Aspartic Acid)
19. Valine (Valine)
20. Hydroxylysine (Hyl)
21. Hydroxyproline (Hydroxyproline)
22. Histidine (Histidine)
23. Glycine (Glycine)
24. Glutamine (GLN)
25. Glutamic Acid (Glutamic Acid)
26. Homocysteine
27. Homocitrulline (Hcit)
28. Isoleucine (Isoleucine)
29. Carnosine (Carnosine)
30. Leucine (Leucine)
31. Lysine (Lysine)
32. Methionine (Methionine)
33. Ornithine (Ornithine)
34. Pipecolic acid
35. Proline (Proline)
36. Sarcosine (Sarcosine)
37. Serine (Serine)
38. Taurine (Taurine)
39. Tyrosine (Tyrosine)
40. Threonine (Threonine)
41. Tryptophan (Tryptophan)
42. Phenylalanine (Phenylalanine)
43. Phosphoserine (Phosphoserine)
44. Phosphoethanolamine (Pet)
45. Cystathionine (Cystathionine)
46. Cystine (Cystine)
47. Citrulline (Citrulline)
48. Ethanolamine (Eta)
Period of execution
Within 6 days. The specified time does not include the day of biomaterial collection
Biomaterial type