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BBS1 Gene Bardet-Biedl Syndrome Type 1 Genetic Test Cost

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

-21%

The BBS1 gene Bardet-Biedl Syndrome Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the BBS1 gene, which are linked to Bardet-Biedl Syndrome (BBS) Type 1. BBS is a rare, genetically inherited disorder characterized by symptoms such as vision loss, kidney dysfunction, obesity, learning disabilities, and extra fingers or toes. Early and accurate diagnosis through genetic testing is crucial for managing the condition and improving the quality of life for affected individuals.

This test specifically looks for alterations in the BBS1 gene, one of the most common genes associated with the condition, to confirm a diagnosis of Bardet-Biedl Syndrome Type 1. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities.

The cost of the BBS1 Gene Bardet-Biedl Syndrome Type 1 Genetic Test at DNA Labs UAE is set at 4400 AED. This cost includes the full process of sample collection, genetic analysis, and the provision of a detailed report by healthcare professionals. The test is an invaluable resource for families with a history of BBS, providing them with essential information for making informed health and lifestyle decisions.

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BBS1 Gene Bardet-Biedl Syndrome Type 1 Genetic Test

Welcome to DNA Labs UAE’s blog on the BBS1 Gene Bardet-Biedl Syndrome Type 1 Genetic Test. In this blog, we will discuss the cost, symptoms, diagnosis, and other important details about this genetic test.

Test Name: BBS1 Gene Bardet-Biedl Syndrome Type 1 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 BBS1 Gene Bardet-Biedl Syndrome Type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS1 Gene Bardet-Biedl Syndrome Type 1 NGS Genetic DNA Test gene BBS1.

Test Details:

The BBS1 gene is associated with Bardet-Biedl Syndrome Type 1 (BBS1), which is a rare genetic disorder characterized by a wide range of symptoms including obesity, vision loss, kidney abnormalities, intellectual disability, and various other physical and developmental abnormalities.

NGS (Next-Generation Sequencing) genetic testing refers to a method of genetic testing that allows for the analysis of multiple genes simultaneously. It is a high-throughput and cost-effective approach that can provide comprehensive genetic information.

The BBS1 gene NGS genetic test specifically analyzes the BBS1 gene for any mutations or variations that may be associated with Bardet-Biedl Syndrome Type 1. This test can help in confirming a diagnosis of BBS1 and can also be used for carrier testing and prenatal testing in families with a known BBS1 gene mutation.

It is important to note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and guidance based on the test results.

Test Name BBS1 Gene Bardet-Biedl syndrome type 1 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 BBS1 Gene Bardet-Biedl syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS1 Gene Bardet-Biedl syndrome type 1 NGS Genetic DNA Test gene BBS1
Test Details

The BBS1 gene is associated with Bardet-Biedl syndrome type 1 (BBS1), which is a rare genetic disorder characterized by a wide range of symptoms including obesity, vision loss, kidney abnormalities, intellectual disability, and various other physical and developmental abnormalities.

NGS (Next-Generation Sequencing) genetic testing refers to a method of genetic testing that allows for the analysis of multiple genes simultaneously. It is a high-throughput and cost-effective approach that can provide comprehensive genetic information.

The BBS1 gene NGS genetic test specifically analyzes the BBS1 gene for any mutations or variations that may be associated with Bardet-Biedl syndrome type 1. This test can help in confirming a diagnosis of BBS1 and can also be used for carrier testing and prenatal testing in families with a known BBS1 gene mutation.

It is important to note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and guidance based on the test results.