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PROK2 Gene Kallmann Syndrome Type 4 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The PROK2 Gene Kallmann Syndrome Type 4 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the PROK2 gene, which are linked to the development of Kallmann Syndrome Type 4. This rare genetic disorder is characterized by a combination of delayed or absent puberty and an impaired sense of smell (anosmia) or a reduced sense of smell (hyposmia). The condition is part of a group of syndromes that affect the production of hormones responsible for sexual development.

The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. By examining the patient’s DNA, the test aims to detect specific mutations in the PROK2 gene that are known to cause Kallmann Syndrome Type 4. This information is crucial for confirming a diagnosis, which can then guide treatment options and genetic counseling for affected individuals and their families.

The cost of the PROK2 Gene Kallmann Syndrome Type 4 Genetic Test is 4400 AED. While the price may seem high, the test offers valuable insights into the genetic basis of the condition, enabling targeted interventions and support for those affected by this syndrome.

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PROK2 Gene Kallmann syndrome type 4 Genetic Test

At DNA Labs UAE, we offer the PROK2 Gene Kallmann syndrome type 4 Genetic Test at a cost of AED 4400.0. This test is designed to diagnose Kallmann syndrome type 4, a rare genetic disorder characterized by delayed or absent puberty and an impaired sense of smell.

Test Components and Price

Test Name: PROK2 Gene Kallmann syndrome type 4 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery

The report for the PROK2 Gene Kallmann syndrome type 4 Genetic Test will be delivered within 3 to 4 weeks.

Method

The test utilizes NGS (Next-Generation Sequencing) Technology for analysis.

Test Type

The PROK2 Gene Kallmann syndrome type 4 Genetic Test falls under the category of Dysmorphology.

Doctor and Test Department

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the PROK2 Gene Kallmann syndrome type 4 NGS Genetic DNA Test. A genetic counseling session may be conducted to draw a pedigree chart of family members affected by the PROK2 gene.

Test Details

The PROK2 gene is associated with Kallmann syndrome type 4. NGS Genetic Test is a high-throughput sequencing technology used to analyze multiple genes or the entire genome. In the case of Kallmann syndrome type 4, the NGS genetic test involves sequencing the PROK2 gene to identify any mutations or variations that may be causing the disorder.

The NGS genetic test for Kallmann syndrome type 4 serves several purposes:

  • Diagnosing the condition
  • Predicting the risk of passing it on to future generations
  • Guiding treatment decisions
  • Providing valuable information for genetic counseling and family planning

It is essential to consult with a healthcare professional or genetic counselor to determine if an NGS genetic test for Kallmann syndrome type 4 is appropriate and to understand the potential implications of the test results.

Test Name PROK2 Gene Kallmann syndrome type 4 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PROK2 Gene Kallmann syndrome type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PROK2 Gene Kallmann syndrome type 4 NGS Genetic DNA Test gene PROK2
Test Details

The PROK2 gene is associated with Kallmann syndrome type 4. Kallmann syndrome is a rare genetic disorder characterized by delayed or absent puberty and an impaired sense of smell. It is caused by mutations in various genes, including PROK2.

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses high-throughput sequencing technologies to rapidly and efficiently analyze multiple genes or the entire genome. In the context of Kallmann syndrome type 4, an NGS genetic test would involve sequencing the PROK2 gene to identify any mutations or variations that may be causing the disorder.

The NGS genetic test for Kallmann syndrome type 4 can help in diagnosing the condition, predicting the risk of passing it on to future generations, and guiding treatment decisions. It can also provide valuable information for genetic counseling and family planning.

It is important to consult with a healthcare professional or genetic counselor to determine if an NGS genetic test for Kallmann syndrome type 4 is appropriate and to understand the potential implications of the test results.

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