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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 tool available at DNA Labs UAE, designed to detect mutations in the PROK2 gene, which are associated with Kallmann Syndrome Type 4. Kallmann Syndrome is a genetic condition characterized by the combination of delayed or absent puberty and an impaired sense of smell (anosmia). Type 4 of this syndrome, specifically linked to mutations in the PROK2 gene, highlights the importance of genetic testing for accurate diagnosis and management.

This test is crucial for individuals displaying symptoms of Kallmann Syndrome or those with a family history of the condition, as it provides definitive genetic evidence of the syndrome. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of genetic mutations in the PROK2 gene.

The cost of the PROK2 Gene Kallmann Syndrome Type 4 Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to identify the genetic alterations responsible for the condition, offering a pathway towards personalized treatment and management strategies for affected individuals. By pinpointing the genetic basis of the syndrome, healthcare providers can offer targeted advice and interventions, significantly improving the quality of life for those diagnosed with Kallmann Syndrome Type 4.

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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

Hepatology Nephrology Endocrinology Disorders

Doctor

General Physician

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, a rare genetic disorder characterized by delayed or absent puberty and an impaired sense of smell (anosmia or hyposmia). Kallmann syndrome is caused by a disruption in the normal development of the hypothalamus, which affects the production and release of hormones involved in sexual development. NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Kallmann syndrome type 4, an NGS genetic test can be performed to identify any variations or mutations in the PROK2 gene. The NGS genetic test involves extracting DNA from a blood or saliva sample and sequencing the entire coding region of the PROK2 gene. This allows for a comprehensive analysis of the gene, including any potential disease-causing mutations or variations. By identifying mutations in the PROK2 gene, the NGS genetic test can confirm a diagnosis of Kallmann syndrome type 4. This information is important for genetic counseling and can help guide treatment decisions for affected individuals.

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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
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, a rare genetic disorder characterized by delayed or absent puberty and an impaired sense of smell (anosmia or hyposmia). Kallmann syndrome is caused by a disruption in the normal development of the hypothalamus, which affects the production and release of hormones involved in sexual development.

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Kallmann syndrome type 4, an NGS genetic test can be performed to identify any variations or mutations in the PROK2 gene.

The NGS genetic test involves extracting DNA from a blood or saliva sample and sequencing the entire coding region of the PROK2 gene. This allows for a comprehensive analysis of the gene, including any potential disease-causing mutations or variations.

By identifying mutations in the PROK2 gene, the NGS genetic test can confirm a diagnosis of Kallmann syndrome type 4. This information is important for genetic counseling and can help guide treatment decisions for affected individuals.

SKU: TEST-3693 Category:

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