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Prader-Willi/Angelman syndrome (MS-MLPA)
SKU: MD-NLMM058 Categories: , , , , , , , , , Tags: , , , , , , ,

In Stock

Prader-Willi/Angelman syndrome (MS-MLPA)

฿12,236.00

Additional information

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

Detects methylation abnormalities associated with Prader-Willi and Angelman syndromes using MS-MLPA.

Product tags: Angelman Syndrome Genetic Test, Developmental Disorders, Family History, Genetic Disorders, Hypotonia, MS-MLPA for Prader-Willi/Angelman, Obesity, Prader-Willi Syndrome Test
Diseases: Developmental Disorders, Genetic Disorders
Symptoms: Hypotonia, Obesity
Habits: Family History
Age Groups: Children, Infants
Specimens: EDTA Whole Blood
Diagnostic Methods: MS-MLPA
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Description

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.

Additional information

Also Known As

Specimen

Turnaround Time

Test Code

Test Type

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