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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

The maximum days the report can be obtained for the test Leptin Deficiency (LEP) Gene Analysis Test is 14 days.

What are the prerequisites for the test Leptin Deficiency (LEP) Gene Analysis Test

  • Physician's order
  • Completed requisition form
  • Consent form signed by the patient or legal guardian
  • Payment for the test (if not covered by insurance)
  • Fast for at least 8 hours before the test
  • Inform the healthcare provider about any medications or supplements being taken

What are the measure values for the test Leptin Deficiency (LEP) Gene Analysis Test

  • Test Name: Leptin Deficiency (LEP) Gene Analysis Test
  • Measure Values:
    • Presence of mutations in the LEP gene
    • Genetic predisposition to leptin deficiency
    • Risk factors for obesity and related health conditions

What does this test Leptin Deficiency (LEP) Gene Analysis Test identify?

  • This test identifies mutations in the Leptin Deficiency (LEP) gene.
  • Leptin is a hormone that plays a key role in regulating energy balance and body weight.
  • Deficiencies in the LEP gene can lead to leptin deficiency, which can result in severe obesity and other metabolic disorders.
  • Identifying mutations in the LEP gene can help healthcare providers diagnose and manage conditions related to leptin deficiency.

Why is this test Leptin Deficiency (LEP) Gene Analysis Test taken?

Leptin Deficiency (LEP) Gene Analysis Test

The Leptin Deficiency (LEP) Gene Analysis Test is taken to determine if an individual has a mutation in the LEP gene that results in a deficiency of leptin production. Leptin is a hormone that plays a key role in regulating energy balance and body weight. A deficiency of leptin can lead to severe obesity and other metabolic disorders.

This test is typically recommended for individuals who have unexplained obesity or who have a family history of leptin deficiency. By identifying a mutation in the LEP gene, healthcare providers can develop personalized treatment plans to help manage the condition and prevent complications.

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