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Requisites
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

Maximum Days for Report: The report for the MS Prader Willi Syndrome (PWS) Test can be obtained within 10-14 business days from the date of sample collection.

What are the prerequisites for the test MS Prader Willi Syndrome (PWS) Test

  • Confirmation of clinical suspicion of Prader-Willi Syndrome (PWS)
  • Genetic counseling and informed consent
  • Collection of a blood sample from the individual
  • Submission of the blood sample to a certified genetic testing laboratory
  • Payment for the test (if not covered by insurance)

What are the measure values for the test MS Prader Willi Syndrome (PWS) Test

Measure Value
Chromosome 15 Deletion Positive or Negative
Methylation Analysis Positive or Negative
Parental Origin Testing Positive or Negative

What does this test MS Prader Willi Syndrome (PWS) Test identify?

MS Prader Willi Syndrome (PWS) Test

The MS Prader Willi Syndrome (PWS) Test is a diagnostic test that identifies a rare genetic disorder called Prader-Willi Syndrome (PWS). This syndrome is characterized by a variety of physical, mental, and behavioral symptoms, including severe obesity, cognitive disabilities, and behavioral problems.

The test analyzes the DNA of the individual to look for specific genetic abnormalities associated with PWS. These abnormalities include the deletion of a segment of chromosome 15, maternal uniparental disomy (both copies of chromosome 15 inherited from the mother), or imprinting defects.

By identifying these genetic abnormalities, the MS Prader Willi Syndrome (PWS) Test can help healthcare providers diagnose PWS early, which is important for starting appropriate treatments and interventions to manage the symptoms of the disorder.

Why is this test MS Prader Willi Syndrome (PWS) Test taken?

The MS Prader Willi Syndrome (PWS) Test is taken to diagnose Prader-Willi Syndrome, a genetic disorder that affects appetite, growth, metabolism, cognitive function, and behavior. This test is usually recommended when a healthcare provider suspects a person may have PWS based on their symptoms and medical history. The test involves analyzing the DNA of the individual to look for specific genetic abnormalities associated with PWS. Early diagnosis of PWS is important for managing the symptoms and providing appropriate care and support to individuals with this condition.

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