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CCDC28B Gene Bardet-Biedl Syndrome Modifier of CCDC28B Related Genetic Test

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

-21%

The CCDC28B gene plays a crucial role as a modifier in the manifestation of Bardet-Biedl Syndrome (BBS), a complex genetic disorder characterized by symptoms such as vision loss, obesity, kidney dysfunction, and extra fingers or toes. The identification of the CCDC28B gene’s involvement has opened avenues for more targeted genetic testing, offering insights into the specific genetic makeup and potential severity of the syndrome in affected individuals.

DNA Labs UAE offers a specialized genetic test focused on the CCDC28B gene to determine its influence on the Bardet-Biedl Syndrome. This test is particularly valuable for individuals diagnosed with BBS or those with a family history of the syndrome, as it can provide critical information regarding prognosis, potential complications, and the most effective management strategies.

The cost of the CCDC28B-related genetic test at DNA Labs UAE is 4400 AED. The test involves a detailed analysis of the CCDC28B gene to identify any mutations or variants that may impact the course of Bardet-Biedl Syndrome. By opting for this test, patients and their families can gain a deeper understanding of their condition, enabling more informed decisions about their healthcare and lifestyle adjustments necessary to manage the syndrome effectively.

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CCDC28B Gene Bardet-Biedl syndrome modifier of CCDC28B related Genetic Test

Components:

  • Test Name: CCDC28B Gene Bardet-Biedl syndrome modifier of CCDC28B related 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 CCDC28B Gene Bardet-Biedl syndrome, modifier of, CCDC28B related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CCDC28B Gene Bardet-Biedl syndrome, modifier of, CCDC28B related NGS Genetic DNA Test gene CCDC28B.

Test Details:

The CCDC28B gene is associated with Bardet-Biedl syndrome, a rare genetic disorder characterized by a wide range of symptoms including obesity, vision problems, kidney abnormalities, and intellectual disability. The CCDC28B gene is involved in the formation and function of cilia, which are hair-like structures found on the surface of cells. Cilia play important roles in various cellular processes, including signal transduction and cell movement.

A modifier of CCDC28B refers to another gene or genetic variant that can influence the severity or presentation of Bardet-Biedl syndrome in individuals with mutations in the CCDC28B gene. Modifiers can either worsen or improve the symptoms of the syndrome.

A CCDC28B related NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the CCDC28B gene and detect any mutations or variants that may be present. This test can help confirm a diagnosis of Bardet-Biedl syndrome in individuals suspected to have the disorder based on their symptoms. It can also provide information about the specific genetic variant in the CCDC28B gene, which can be useful for genetic counseling and family planning.

Test Name CCDC28B Gene Bardet-Biedl syndrome modifier of CCDC28B related 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 CCDC28B Gene Bardet-Biedl syndrome, modifier of, CCDC28B related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CCDC28B Gene Bardet-Biedl syndrome, modifier of, CCDC28B related NGS Genetic DNA Test gene CCDC28B
Test Details

The CCDC28B gene is associated with Bardet-Biedl syndrome, a rare genetic disorder characterized by a wide range of symptoms including obesity, vision problems, kidney abnormalities, and intellectual disability. The CCDC28B gene is involved in the formation and function of cilia, which are hair-like structures found on the surface of cells. Cilia play important roles in various cellular processes, including signal transduction and cell movement.

A modifier of CCDC28B refers to another gene or genetic variant that can influence the severity or presentation of Bardet-Biedl syndrome in individuals with mutations in the CCDC28B gene. Modifiers can either worsen or improve the symptoms of the syndrome.

A CCDC28B related NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the CCDC28B gene and detect any mutations or variants that may be present. This test can help confirm a diagnosis of Bardet-Biedl syndrome in individuals suspected to have the disorder based on their symptoms. It can also provide information about the specific genetic variant in the CCDC28B gene, which can be useful for genetic counseling and family planning.

SKU: TEST-3584 Category:

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