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Methylation and Deletion/duplication analysis on 11p15.5 region for Beckwith-Wiedemann syndrome (CGC genetics)
SKU: MD-NLMA352 Categories: , , , , , , , , , , Tags: , , , , , ,

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Methylation and Deletion/duplication analysis on 11p15.5 region for Beckwith-Wiedemann syndrome (CGC genetics)

฿39,520.00

Additional information

Also Known As

Beckwith-Wiedemann Syndrome Testing
Specimen

1. Peripheral blood (EDTA) 3 mL or 2. Amniotic fluid 5 mL in Sterile tube
Turnaround Time

40 days
Test Code

MD-NLMA352
Test Type

Special
Related Tests

Genetic Disease Panel, Overgrowth Syndrome Testing

Detects methylation abnormalities and deletions/duplications in the 11p15.5 region associated with Beckwith-Wiedemann syndrome, a genetic overgrowth disorder.

Product tags: Beckwith-Wiedemann Syndrome, Beckwith-Wiedemann Syndrome Testing, Genetic Disorders, Hypoglycemia, None, Organ Enlargement, Overgrowth
Diseases: Beckwith-Wiedemann Syndrome, Genetic Disorders
Symptoms: Hypoglycemia, Organ Enlargement, Overgrowth
Habits: None
Age Groups: Pediatrics
Specimens: Amniotic Fluid, EDTA Whole Blood
Diagnostic Methods: Methylation and Deletion/Duplication Analysis
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Description

Detects methylation abnormalities and deletions/duplications in the 11p15.5 region associated with Beckwith-Wiedemann syndrome, a genetic overgrowth disorder.

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

Beckwith-Wiedemann Syndrome Testing
Specimen

1. Peripheral blood (EDTA) 3 mL or 2. Amniotic fluid 5 mL in Sterile tube
Turnaround Time

40 days
Test Code

MD-NLMA352
Test Type

Special
Related Tests

Genetic Disease Panel, Overgrowth Syndrome Testing

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