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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 Turnaround Time for Kallmann Syndrome Gene Panel Test Report

The report for the Kallmann Syndrome Gene Panel test can be obtained within 14-21 business days from the date of sample collection.

What are the prerequisites for the test Kallmann Syndrome Gene Panel

Prerequisites for the Kallmann Syndrome Gene Panel Test

Prerequisites for the Kallmann Syndrome Gene Panel Test

  • Referral from a healthcare provider
  • Confirmation of clinical suspicion of Kallmann syndrome
  • Consent form signed by the patient or legal guardian
  • Complete medical history and family history provided
  • Insurance verification and pre-authorization if applicable

What are the measure values for the test Kallmann Syndrome Gene Panel

Gene Measure Values
KAL1 0-1
FGFR1 0-1
PROK2 0-1
PROKR2 0-1

What does this test Kallmann Syndrome Gene Panel identify?

  • Kallmann Syndrome Gene Panel identifies mutations in genes associated with Kallmann Syndrome, a rare genetic disorder characterized by delayed or absent puberty and a lack of sense of smell.
  • The panel typically includes genes such as ANOS1, FGFR1, FGF8, PROKR2, PROK2, CHD7, and others that are known to be involved in the development of the hypothalamus and olfactory system.
  • Identifying mutations in these genes can help confirm a diagnosis of Kallmann Syndrome and provide information about the specific genetic cause of the condition.

Why is this test Kallmann Syndrome Gene Panel taken?

The Kallmann Syndrome Gene Panel test is taken to diagnose Kallmann syndrome, a rare genetic disorder that affects the development of the hypothalamus, a region of the brain that controls the production of hormones. This syndrome is characterized by delayed or absent puberty and an impaired sense of smell (anosmia). The gene panel test analyzes specific genes associated with Kallmann syndrome to identify any mutations or abnormalities that may be causing the disorder.

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