Detects methylation abnormalities associated with Prader-Willi and Angelman syndromes using MS-MLPA…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
Prader-Willi/Angelman syndrome (MS-MLPA)
Detects methylation abnormalities associated with Prader-Willi and Angelman syndromes using MS-MLPA.
12,236 THB
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Lab Categories : Children, Developmental Disorders, EDTA Whole Blood, Family History, Genetic Disorders, Hypotonia, Infants, Lab Test, MS-MLPA, Obesity
Diseases : Developmental Disorders, Genetic Disorders
Habits : Family History
Specimens : EDTA Whole Blood
Diagnostic Methods : MS-MLPA
| Also Known As | Prader-Willi Syndrome Test, Angelman Syndrome Genetic Test, MS-MLPA for Prader-Willi/Angelman |
|---|---|
| Specimen | EDTA whole blood 3-5 ml. |
| Turnaround Time | 21 Days |
| Test Code | MD-NLMM058 |
| Test Type | Special |
| Related Tests | Genetic Disorder Panel |
