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BBS12 Gene Bardet-Biedl Syndrome Type 12 Genetic Test

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

-21%

The BBS12 Gene Bardet-Biedl Syndrome Type 12 Genetic Test is a specialized diagnostic examination designed to identify mutations in the BBS12 gene, which are associated with Bardet-Biedl Syndrome (BBS) Type 12. BBS is a complex genetic condition characterized by symptoms such as vision loss, kidney dysfunction, obesity, learning disabilities, and extra fingers or toes. The BBS12 gene plays a critical role in cell functioning and structure, and mutations in this gene can lead to the development of the syndrome.

Conducted at DNA Labs UAE, this test is a crucial tool for individuals with a family history of BBS or those exhibiting symptoms of the syndrome, offering them a definitive diagnosis. By analyzing a sample of the patient’s DNA, the test can detect specific genetic alterations in the BBS12 gene, confirming the presence of Bardet-Biedl Syndrome Type 12.

The cost of the BBS12 Gene Bardet-Biedl Syndrome Type 12 Genetic Test is 4400 AED. While the price may seem significant, the test provides invaluable information for the management and treatment of the syndrome, potentially improving the quality of life for those affected. Early diagnosis through genetic testing allows for timely intervention, including specialized care and support, to address the various health issues associated with BBS.

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BBS12 Gene Bardet-Biedl Syndrome Type 12 Genetic Test

Cost: AED 4400.0

Test Components:

  • Price: AED 4400.0
  • 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 BBS12 Gene Bardet-Biedl Syndrome Type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS12 Gene Bardet-Biedl Syndrome Type 12 NGS Genetic DNA Test gene BBS12.

Test Details:

The BBS12 gene is associated with Bardet-Biedl Syndrome Type 12, a rare genetic disorder characterized by a variety of symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes). NGS (Next-Generation Sequencing) genetic testing is a method used to analyze and sequence a person’s DNA to identify any genetic variations or mutations that may be present in the BBS12 gene.

This test can help confirm a diagnosis of Bardet-Biedl Syndrome Type 12 and provide information about the specific genetic changes that may be causing the condition. It can also be used for carrier testing and prenatal diagnosis in families with a known BBS12 gene mutation.

Test Name BBS12 Gene Bardet-Biedl syndrome type 12 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 BBS12 Gene Bardet-Biedl syndrome type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS12 Gene Bardet-Biedl syndrome type 12 NGS Genetic DNA Test gene BBS12
Test Details

The BBS12 gene is associated with Bardet-Biedl syndrome type 12, a rare genetic disorder characterized by a variety of symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze and sequence a person’s DNA to identify any genetic variations or mutations that may be present in the BBS12 gene. This test can help confirm a diagnosis of Bardet-Biedl syndrome type 12 and provide information about the specific genetic changes that may be causing the condition. It can also be used for carrier testing and prenatal diagnosis in families with a known BBS12 gene mutation.