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RAB3GAP2 Gene Martsolf Syndrome Genetic Test Cost

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

-21%

The RAB3GAP2 gene plays a crucial role in the development and function of various systems in the body. Mutations in this gene are associated with Martsolf syndrome, a rare genetic disorder characterized by intellectual disability, cataracts, hypogonadism, and other physical abnormalities. To diagnose this condition, genetic testing of the RAB3GAP2 gene is essential.

DNA Labs UAE offers a specialized genetic test for Martsolf syndrome by analyzing the RAB3GAP2 gene. This test is crucial for confirming the diagnosis, understanding the severity of the condition, and guiding treatment and management decisions. The test is performed using a sample of the patient’s blood or saliva, employing advanced genetic sequencing technologies to detect mutations in the RAB3GAP2 gene.

The cost of the RAB3GAP2 gene test for Martsolf syndrome at DNA Labs UAE is 4400 AED. This price includes the collection of the sample, the genetic analysis, and a comprehensive report that explains the results. The report is invaluable for healthcare providers in planning the best course of action for patients with Martsolf syndrome and for families to understand the genetic basis of the condition.

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
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RAB3GAP2 Gene Martsolf syndrome 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 RAB3GAP2 Gene Martsolf syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAB3GAP2 Gene Martsolf syndrome NGS Genetic DNA Test gene RAB3GAP2.

Test Details

The RAB3GAP2 gene is associated with Martsolf syndrome, which is a rare genetic disorder characterized by intellectual disability, developmental delay, hearing loss, and other physical abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. In the case of Martsolf syndrome, NGS genetic testing can be used to identify mutations or variations in the RAB3GAP2 gene that may be causing the disorder. This can help with diagnosis, genetic counseling, and potentially guiding treatment options for affected individuals and their families.

Test Name RAB3GAP2 Gene Martsolf syndrome 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 RAB3GAP2 Gene Martsolf syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAB3GAP2 Gene Martsolf syndrome NGS Genetic DNA Test gene RAB3GAP2
Test Details

The RAB3GAP2 gene is associated with Martsolf syndrome, which is a rare genetic disorder characterized by intellectual disability, developmental delay, hearing loss, and other physical abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. In the case of Martsolf syndrome, NGS genetic testing can be used to identify mutations or variations in the RAB3GAP2 gene that may be causing the disorder. This can help with diagnosis, genetic counseling, and potentially guiding treatment options for affected individuals and their families.