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Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

Test Name:
Rett Syndrome (MECP2) Deletion/Duplication Analysis Test
Maximum Turnaround Time:
60 days

What are the prerequisites for the test Rett Syndrome (MECP2) Deletion/Duplication Analysis Test

  • Patient must have symptoms consistent with Rett Syndrome
  • Physician’s order
  • Signed informed consent form
  • Blood or saliva sample from the patient

What are the measure values for the test Rett Syndrome (MECP2) Deletion/Duplication Analysis Test

  • Test Name: Rett Syndrome (MECP2) Deletion/Duplication Analysis Test
  • Method: Polymerase Chain Reaction (PCR) and Multiplex Ligation-dependent Probe Amplification (MLPA)
  • Sample Type: Blood or saliva
  • Turnaround Time: 2-4 weeks
  • Test Code: MECP2DDA
  • Test Price: $500

What does this test Rett Syndrome (MECP2) Deletion/Duplication Analysis Test identify?

  • This test identifies deletions or duplications in the MECP2 gene.
  • MECP2 gene is associated with Rett Syndrome, a neurological disorder that primarily affects girls.
  • Deletions or duplications in the MECP2 gene can lead to the development of Rett Syndrome.
  • Identifying these genetic abnormalities can help in diagnosing Rett Syndrome and providing appropriate treatment and management.

Why is this test Rett Syndrome (MECP2) Deletion/Duplication Analysis Test taken?

This test is taken to detect deletions or duplications in the MECP2 gene, which is associated with Rett Syndrome. Rett Syndrome is a rare genetic disorder that primarily affects girls and leads to severe physical and cognitive impairments. By analyzing the MECP2 gene for deletions or duplications, healthcare providers can confirm a diagnosis of Rett Syndrome and provide appropriate treatment and management for the condition. This test is typically recommended for individuals who exhibit symptoms of Rett Syndrome or have a family history of the disorder.

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