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HCRT Gene Narcolepsy Genetic Test Cost

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

-21%

The HCRT Gene Narcolepsy Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the hypocretin (orexin) receptor 2 gene (HCRT), which are strongly associated with the development of narcolepsy. Narcolepsy is a chronic sleep disorder characterized by overwhelming daytime drowsiness and sudden attacks of sleep, often leading to significant disruptions in daily life. This genetic test plays a crucial role in the early detection and diagnosis of narcolepsy, allowing for timely intervention and management of the condition.

Performed in the state-of-the-art facilities of DNA Labs UAE, the test requires a simple blood sample from the patient. The sample is then analyzed for specific genetic markers that indicate a predisposition to narcolepsy. The process is highly accurate, leveraging advanced genetic sequencing techniques to ensure reliable results.

The cost of the HCRT Gene Narcolepsy Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of early detection and the potential for improved quality of life through personalized treatment plans make it a worthwhile investment for individuals experiencing symptoms of narcolepsy or those with a family history of the disorder.

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  • This test is not intended for medical diagnosis or treatment
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HCRT Gene Narcolepsy Genetic Test

Test Name: HCRT Gene Narcolepsy 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for HCRT Gene Narcolepsy NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with HCRT Gene Narcolepsy

Test Details

The HCRT gene is associated with narcolepsy, a neurological disorder characterized by excessive daytime sleepiness, cataplexy (sudden loss of muscle tone), hallucinations, and sleep paralysis.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the context of narcolepsy, NGS genetic testing can be used to identify specific variations or mutations in the HCRT gene that may be associated with the development of narcolepsy.

By analyzing the HCRT gene using NGS technology, healthcare professionals can identify genetic variants that may increase the risk of narcolepsy or help confirm a diagnosis. This information can be valuable in understanding the underlying cause of narcolepsy and potentially guide treatment decisions.

It’s important to note that genetic testing for narcolepsy is not typically used as a standalone diagnostic tool. It is usually performed in combination with other clinical assessments and sleep studies to make an accurate diagnosis. Additionally, not all individuals with narcolepsy will have identifiable genetic mutations in the HCRT gene, as there may be other genetic and environmental factors contributing to the disorder.

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

The HCRT gene is associated with narcolepsy, a neurological disorder characterized by excessive daytime sleepiness, cataplexy (sudden loss of muscle tone), hallucinations, and sleep paralysis.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the context of narcolepsy, NGS genetic testing can be used to identify specific variations or mutations in the HCRT gene that may be associated with the development of narcolepsy.

By analyzing the HCRT gene using NGS technology, healthcare professionals can identify genetic variants that may increase the risk of narcolepsy or help confirm a diagnosis. This information can be valuable in understanding the underlying cause of narcolepsy and potentially guide treatment decisions.

It’s important to note that genetic testing for narcolepsy is not typically used as a standalone diagnostic tool. It is usually performed in combination with other clinical assessments and sleep studies to make an accurate diagnosis. Additionally, not all individuals with narcolepsy will have identifiable genetic mutations in the HCRT gene, as there may be other genetic and environmental factors contributing to the disorder.