Creatine Biosynthesis Testing : Creatine/GAA (Plasma)

Test Information

Creatine biosynthesis disorders can be separated based on urine testing for guanidinoacetate (GAA) and creatine. Patients with AGAT deficiency show a low urinary GAA level while patients with GAMT have an elevated GAA level.

Turnaround Time

2 weeks

CPT Code(s)

82540, 82542

Cost

$148

Clinical Information

Both AGAT and GAMT are autosomal recessive disorders and are characterized by intellectual disability, speech delay and epilepsy. GAMT deficiency can also present with a dystonic hyperkinetic movement disorder.

Methodology

tandem mass spectrometry (MS-MS)

Specimen Requirements

At least 500ul of plasma is requested for the analysis.

Transport Instructions

Whole blood should be shipped overnight at ambient temperature. Or, the specimen can be spun down, plasma removed and frozen. Frozen plasma should be shipped overnight on dry ice.

Have Questions Need Support?

Call our laboratory at 1-800-473-9411 or contact one of our Laboratory Genetic Counselors for assistance.
Robin Fletcher, MS, CGC
Kellie Walden, MS, CGC

Analyte Analysis, Analytes and Biomarkers, Biochemical Testing
Meet Reggie Roper

Meet Reggie Roper

Reggie has been part of the GGC family for over 18 years. He has short stature, webbing of his hands, pulmonary stenosis, seizures and hydrocephalus along with developmental delay. He carried an initial diagnosis of cardiofaciocutaneous (CFC) syndrome; however, as genetic testing advanced, GGC made the diagnosis of Noonan-like syndrome with loose anagen hair by identifying a mutation in the SHOC2 gene. He is also an active participant in the Greenwood Community Theatre's Penguin Project. "GGC is...

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