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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

Maximum days to obtain report for Monogenic & Syndromic Obesity Gene Panel: 60 days

What are the prerequisites for the test Monogenic & Syndromic Obesity Gene Panel

  • Patients with a clinical suspicion of monogenic or syndromic obesity
  • Referral form filled out by a healthcare provider
  • Consent form signed by the patient or legal guardian
  • Payment or insurance information provided

What are the measure values for the test Monogenic & Syndromic Obesity Gene Panel

  1. MC4R gene sequencing
  2. LEP gene sequencing
  3. LEPR gene sequencing
  4. POMC gene sequencing
  5. PCSK1 gene sequencing
  6. BSCL2 gene sequencing
  7. AGRP gene sequencing
  8. SH2B1 gene sequencing

What does this test Monogenic & Syndromic Obesity Gene Panel identify?

  • This test identifies mutations in genes that are associated with monogenic obesity, which is obesity caused by a single gene mutation.
  • It also identifies mutations in genes that are associated with syndromic obesity, which is obesity that is part of a larger genetic syndrome.
  • The test analyzes a panel of genes known to be involved in regulating appetite, energy expenditure, and metabolism, which are all factors that can contribute to obesity.
  • Identifying mutations in these genes can help healthcare providers better understand the underlying cause of a patient's obesity and tailor treatment plans accordingly.

Why is this test Monogenic & Syndromic Obesity Gene Panel taken?

The Monogenic & Syndromic Obesity Gene Panel test is taken to identify genetic mutations or variations that may be responsible for monogenic or syndromic forms of obesity. Monogenic obesity is caused by mutations in a single gene, while syndromic obesity is associated with specific genetic syndromes.

By analyzing a panel of genes associated with monogenic and syndromic obesity, this test can help healthcare providers diagnose the underlying genetic cause of obesity in individuals who have a strong family history of obesity or who exhibit unusual symptoms or features associated with genetic syndromes.

Understanding the genetic basis of obesity can help guide treatment options and personalized management plans for individuals with monogenic or syndromic forms of obesity.

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