Sale!

DHH Gene 46XY gonadal dysgenesis partial with minifascicular neuropathy Genetic Test

4,400 د.إ

-21%

The “DHH Gene 46XY Gonadal Dysgenesis Partial with Minifascicular Neuropathy Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, aimed at detecting mutations in the DHH gene that are associated with 46XY gonadal dysgenesis partial syndrome accompanied by minifascicular neuropathy. This condition is characterized by underdeveloped gonads in individuals who are genetically male (with one X and one Y chromosome), leading to a range of developmental and reproductive issues. Additionally, the presence of minifascicular neuropathy indicates a neurological component, where nerve fibers are abnormally organized into small bundles or fascicles, potentially causing sensory and motor deficits.

The test is critical for early diagnosis and management of the condition, enabling healthcare providers to offer appropriate treatments and interventions to improve the quality of life of affected individuals. The cost of the test is set at 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive insights it provides into the patient’s condition. By conducting this test at DNA Labs UAE, patients and their families can access advanced genetic testing services within the region, supported by a team of experts in genetics and molecular diagnostics.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

DHH Gene 46XY Gonadal Dysgenesis Partial with Minifascicular Neuropathy Genetic Test

Genetic testing plays a crucial role in identifying and diagnosing various genetic disorders. One such test is the DHH Gene 46XY gonadal dysgenesis partial with minifascicular neuropathy Genetic Test.

Test Components and Price

The DHH Gene 46XY gonadal dysgenesis partial with minifascicular neuropathy Genetic Test costs AED 4400.0. The test components include:

  • 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

Before undergoing the DHH Gene 46XY gonadal dysgenesis partial with minifascicular neuropathy Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by this condition.

Test Details

The DHH gene is associated with 46XY gonadal dysgenesis partial with minifascicular neuropathy. This condition is characterized by incomplete development of the testes in individuals with male chromosomes (46,XY), leading to infertility and reduced testosterone production. It is also linked to minifascicular neuropathy, a type of neuropathy that causes muscle weakness and atrophy in the hands and feet.

The DHH Gene 46XY gonadal dysgenesis partial with minifascicular neuropathy Genetic Test utilizes next-generation sequencing (NGS) technology to analyze the DNA sequence of the DHH gene. This allows for the detection of any changes or mutations that may be present. The information obtained from this test can be used for diagnosis, genetic counseling, and treatment planning.

Test Name DHH Gene 46XY gonadal dysgenesis partial with minifascicular neuropathy 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 DHH Gene 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DHH Gene 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy
Test Details

The DHH gene is associated with 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy. This condition is characterized by incomplete development of the testes in individuals with male chromosomes (46,XY) resulting in infertility and reduced production of testosterone. It is also associated with a form of neuropathy known as minifascicular neuropathy, which causes muscle weakness and atrophy in the hands and feet.

NGS genetic testing can identify mutations in the DHH gene that are associated with this condition. This test uses next-generation sequencing technology to analyze the DNA sequence of the gene and detect any changes or mutations that may be present. This information can be used to diagnose the condition, provide genetic counseling, and guide treatment options.