Referred Tests
| Web: | mayocliniclabs.com |
|---|---|
| Email: | mcl@mayo.edu |
| Telephone: | 800-533-1710 |
| International: | +1 855-379-3115 |
| Values are valid only on day of printing. | |
Test ID: SSCTU
S-Sulfocysteine Panel, Urine
Useful For 
Suggests clinical disorders or settings where the test may be helpful
Diagnosis of molybdenum cofactor deficiency, isolated sulfite oxidase deficiency and hereditary xanthinuria
Monitoring patients with molybdenum cofactor deficiency or isolated sulfite oxidase deficiency on treatment
Highlights
This test provides a quantitative report of S-sulfocysteine, xanthine, hypoxanthine and uric acid identified via liquid chromatography-mass spectrometry.
Method Name A short description of the method used to perform the test
Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)
NY State Available Indicates the status of NY State approval and if the test is orderable for NY State clients.
Yes
Reporting Name Lists a shorter or abbreviated version of the Published Name for a test
S-Sulfocysteine Panel, U
Aliases Lists additional common names for a test, as an aid in searching
Hypoxanthine
S-Sulfocysteine
Uric Acid
Xanthine
Hereditary xanthinuria
Isolated sulfite oxidase deficiency
Lesch-Nyhan syndrome
Molybdenum cofactor deficiency
Xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency
Xanthine dehydrogenase deficiency
Xanthine dehydrogenase/xanthine aldehyde oxidase/sulfite oxidase combined deficiency
S-Sulfocysteine
Uric Acid
Xanthine
Hereditary xanthinuria
Isolated sulfite oxidase deficiency
Lesch-Nyhan syndrome
Molybdenum cofactor deficiency
Xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency
Xanthine dehydrogenase deficiency
Xanthine dehydrogenase/xanthine aldehyde oxidase/sulfite oxidase combined deficiency