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BBS7 Gene Bardet-Biedl Syndrome Type 7 Genetic Test

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

-21%

The Bardet-Biedl Syndrome Type 7 (BBS7) Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the BBS7 gene, which are implicated in Bardet-Biedl Syndrome (BBS). This rare, autosomal recessive genetic disorder is characterized by symptoms such as retinal degeneration, obesity, polydactyly, renal abnormalities, and cognitive impairment. The test, priced at 4400 AED, plays a crucial role in the early detection and management of BBS, enabling healthcare providers to devise personalized treatment plans and offer genetic counseling to affected families. By identifying specific genetic mutations associated with the syndrome, the BBS7 Genetic Test aids in the accurate diagnosis of BBS, facilitating early interventions and improving patient outcomes.

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BBS7 Gene Bardet-Biedl syndrome type 7 Genetic Test

Are you concerned about Bardet-Biedl syndrome type 7 (BBS7)? DNA Labs UAE offers a comprehensive genetic test that can provide valuable insights into this rare genetic disorder.

Test Name: BBS7 Gene Bardet-Biedl syndrome type 7 Genetic Test

  • Components: BBS7 gene analysis
  • 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

Prior to undergoing the BBS7 Gene Bardet-Biedl syndrome type 7 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by BBS7 Gene Bardet-Biedl syndrome type 7 NGS Genetic DNA Test gene BBS7.

Test Details

The BBS7 gene is associated with Bardet-Biedl syndrome type 7 (BBS7), a rare genetic disorder characterized by symptoms such as obesity, retinal degeneration, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes).

NGS (Next-Generation Sequencing) genetic testing is a powerful tool that allows for the simultaneous analysis of multiple genes. In the case of BBS7, NGS genetic testing can identify mutations or variations in the BBS7 gene, which may be responsible for the development of Bardet-Biedl syndrome type 7.

NGS genetic testing provides valuable information for diagnosis, prognosis, and genetic counseling. It can also be used for carrier testing and prenatal testing in families with a known BBS7 mutation. However, it is important to note that NGS genetic testing should be performed by specialized laboratories and ordered and interpreted by healthcare professionals with expertise in genetics.

Genetic counseling is highly recommended both before and after genetic testing to ensure individuals and families fully understand the implications of the test results.

Test Name BBS7 Gene Bardet-Biedl syndrome type 7 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 BBS7 Gene Bardet-Biedl syndrome type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS7 Gene Bardet-Biedl syndrome type 7 NGS Genetic DNA Test gene BBS7
Test Details

The BBS7 gene is associated with Bardet-Biedl syndrome type 7 (BBS7), which is a rare genetic disorder characterized by a variety of symptoms including obesity, retinal degeneration, kidney abnormalities, intellectual disability, and polydactyly (extra fingers or toes).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of BBS7, NGS genetic testing can be used to identify mutations or variations in the BBS7 gene that may be responsible for the development of Bardet-Biedl syndrome type 7.

NGS genetic testing can provide valuable information for diagnosis, prognosis, and genetic counseling for individuals suspected of having or being at risk for Bardet-Biedl syndrome type 7. It can also be used for carrier testing and prenatal testing in families with a known BBS7 mutation.

It’s important to note that NGS genetic testing is typically performed by specialized laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetics. Genetic counseling is also recommended before and after genetic testing to help individuals and families understand the implications of the test results.