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MKS1 Gene Bardet-Biedl Syndrome Type 13 Genetic Test Cost

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

-21%

The MKS1 Gene Bardet-Biedl Syndrome Type 13 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the MKS1 gene, which are linked to Bardet-Biedl Syndrome (BBS) Type 13. BBS is a rare genetic disorder that affects multiple body systems, leading to symptoms such as vision loss, obesity, kidney dysfunction, and polydactyly, among others. The test plays a crucial role in the early detection and management of this condition, enabling healthcare providers to develop personalized treatment plans and offer genetic counseling to affected families. Priced at 4400 AED, this test offers invaluable insights into the genetic basis of Bardet-Biedl Syndrome, facilitating improved patient outcomes through targeted interventions.

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MKS1 Gene Bardet-Biedl Syndrome Type 13 Genetic Test

At DNA Labs UAE, we offer the MKS1 Gene Bardet-Biedl Syndrome Type 13 Genetic Test at a price of 4400.0 AED. This test is used to diagnose Bardet-Biedl syndrome type 13, a rare genetic disorder characterized by symptoms such as obesity, vision loss, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes).

Test Components and Details

  • Test Name: MKS1 Gene Bardet-Biedl Syndrome Type 13 Genetic Test
  • 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 MKS1 Gene Bardet-Biedl Syndrome Type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MKS1 Gene Bardet-Biedl Syndrome Type 13 NGS Genetic DNA Test gene MKS1

About the MKS1 Gene and NGS Genetic Testing

The MKS1 gene is associated with Bardet-Biedl Syndrome Type 13. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic mutations or variants. In the case of Bardet-Biedl Syndrome Type 13, NGS genetic testing can be used to analyze the MKS1 gene for any mutations or variants that may be present.

By identifying specific genetic mutations or variants in the MKS1 gene, NGS genetic testing can help confirm a diagnosis of Bardet-Biedl Syndrome Type 13 and provide information about the specific genetic cause of the disorder. This information can be useful for genetic counseling, family planning, and potentially for the development of targeted treatments in the future.

Test Name MKS1 Gene Bardet-Biedl syndrome type 13 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 MKS1 Gene Bardet-Biedl syndrome type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MKS1 Gene Bardet-Biedl syndrome type 13 NGS Genetic DNA Test gene MKS1
Test Details

The MKS1 gene is associated with Bardet-Biedl syndrome type 13. Bardet-Biedl syndrome is a rare genetic disorder characterized by a combination of symptoms including obesity, vision loss, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic mutations or variants. In the case of Bardet-Biedl syndrome type 13, NGS genetic testing can be used to analyze the MKS1 gene for any mutations or variants that may be present.

By identifying specific genetic mutations or variants in the MKS1 gene, NGS genetic testing can help confirm a diagnosis of Bardet-Biedl syndrome type 13 and provide information about the specific genetic cause of the disorder. This can be useful for genetic counseling, family planning, and potentially for the development of targeted treatments in the future.

SKU: TEST-3572