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BBS10 Gene Bardet-Biedl Syndrome Type 10 Genetic Test Cost

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

-21%

The BBS10 Gene Bardet-Biedl Syndrome Type 10 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the BBS10 gene. This gene is one of the known genetic contributors to Bardet-Biedl Syndrome (BBS), a complex disorder that affects multiple body systems. BBS is characterized by symptoms such as retinal dystrophy, obesity, polydactyly, renal abnormalities, and learning difficulties, among others. The test plays a critical role in the early diagnosis and management of the syndrome, allowing for tailored treatment and intervention strategies.

Performed through a simple blood sample or cheek swab, the test examines the BBS10 gene for specific mutations known to cause the syndrome. The process involves sophisticated genetic sequencing techniques to ensure accurate and reliable results. With a cost of 4400 AED, the test is an investment in the health and well-being of individuals at risk of or suspected to have Bardet-Biedl Syndrome. Early diagnosis through the BBS10 Gene Test can significantly improve the quality of life for affected individuals by enabling proactive management of symptoms and complications associated with the syndrome. DNA Labs UAE stands at the forefront of genetic testing, offering this vital service as part of their comprehensive suite of diagnostic solutions.

Description

BBS10 Gene Bardet-Biedl Syndrome Type 10 Genetic Test

Test Name: BBS10 Gene Bardet-Biedl Syndrome Type 10 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 BBS10 Gene Bardet-Biedl Syndrome Type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS10 Gene Bardet-Biedl Syndrome Type 10 NGS Genetic DNA Test gene BBS10

Test Details: The BBS10 gene is associated with Bardet-Biedl Syndrome Type 10, a rare genetic disorder that affects multiple organ systems. Bardet-Biedl Syndrome is characterized by a range of symptoms including obesity, vision problems, kidney abnormalities, extra fingers or toes, and intellectual disability. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of specific genetic variants or mutations that may be present in an individual’s DNA. In the case of BBS10, NGS genetic testing can be used to detect any mutations or variants in the BBS10 gene that may be causing Bardet-Biedl Syndrome Type 10. This type of genetic testing can be helpful in confirming a diagnosis, providing information about disease progression and potential complications, and guiding treatment and management options. It may also be used for carrier testing in individuals with a family history of Bardet-Biedl Syndrome or for prenatal testing in families at risk of having a child with the condition. It is important to note that genetic testing should always be done in consultation with a healthcare professional or genetic counselor, who can provide guidance and support throughout the testing process and help interpret the results.

Test Name	BBS10 Gene Bardet-Biedl syndrome type 10 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 BBS10 Gene Bardet-Biedl syndrome type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BBS10 Gene Bardet-Biedl syndrome type 10 NGS Genetic DNA Test gene BBS10
Test Details	The BBS10 gene is associated with Bardet-Biedl syndrome type 10, a rare genetic disorder that affects multiple organ systems. Bardet-Biedl syndrome is characterized by a range of symptoms including obesity, vision problems, kidney abnormalities, extra fingers or toes, and intellectual disability. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of specific genetic variants or mutations that may be present in an individual’s DNA. In the case of BBS10, NGS genetic testing can be used to detect any mutations or variants in the BBS10 gene that may be causing Bardet-Biedl syndrome type 10. This type of genetic testing can be helpful in confirming a diagnosis, providing information about disease progression and potential complications, and guiding treatment and management options. It may also be used for carrier testing in individuals with a family history of Bardet-Biedl syndrome or for prenatal testing in families at risk of having a child with the condition. It is important to note that genetic testing should always be done in consultation with a healthcare professional or genetic counselor, who can provide guidance and support throughout the testing process and help interpret the results.