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LZTFL1 Gene Bardet-Biedl Syndrome LZTFL1 Related Genetic Test Cost

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

-21%

The LZTFL1 gene plays a crucial role in the development of Bardet-Biedl Syndrome (BBS), a complex genetic disorder that affects multiple body systems. BBS is characterized by symptoms such as obesity, retinal degeneration, polydactyly, renal abnormalities, and learning difficulties. The condition is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

Understanding the genetic basis of Bardet-Biedl Syndrome has led to the development of specific genetic tests that can identify mutations in the LZTFL1 gene, among others associated with BBS. One such test is available at DNA Labs UAE, a leading provider of genetic testing services in the region. This test specifically looks for mutations in the LZTFL1 gene that are known to contribute to the development of Bardet-Biedl Syndrome.

The test is conducted through a simple and non-invasive procedure, typically involving a blood sample or a buccal swab from the patient. The sample is then analyzed using advanced genetic sequencing techniques to identify any mutations in the LZTFL1 gene.

The cost of the LZTFL1-related genetic test for Bardet-Biedl Syndrome at DNA Labs UAE is 4400 AED. This cost includes the collection of the sample, its analysis, and a comprehensive report that explains the findings. The report is an invaluable tool for patients and their families, providing them with crucial information about the genetic basis of the condition, which can inform treatment decisions and help in managing the syndrome more effectively.

Overall, the availability of genetic testing for Bardet-Biedl Syndrome through the identification of LZTFL1 gene mutations offers hope for affected individuals and their families, providing them with a clearer understanding of the condition and guiding them towards appropriate care and management strategies.

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LZTFL1 Gene Bardet-Biedl Syndrome LZTFL1 Related Genetic Test

Genetic testing plays a crucial role in diagnosing and understanding genetic disorders. One such disorder is Bardet-Biedl syndrome (BBS), a rare genetic disorder with various symptoms including obesity, vision problems, kidney abnormalities, and intellectual disability. DNA Labs UAE offers the LZTFL1 Gene Bardet-Biedl syndrome LZTFL1 related Genetic Test, which focuses on the LZTFL1 gene associated with BBS.

Test Details

The LZTFL1 gene is analyzed using Next-Generation Sequencing (NGS) technology. NGS genetic testing allows for the simultaneous analysis of multiple genes. In the case of LZTFL1 related NGS genetic testing, it specifically looks for any potential genetic variants or mutations in the LZTFL1 gene that may be associated with Bardet-Biedl syndrome.

Components and Price

The cost of the LZTFL1 Gene Bardet-Biedl syndrome LZTFL1 related Genetic Test is 4400.0 AED. The test requires a sample condition of blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The report for the LZTFL1 Gene Bardet-Biedl syndrome LZTFL1 related Genetic Test is typically delivered within 3 to 4 weeks.

Test Type and Department

The LZTFL1 Gene Bardet-Biedl syndrome LZTFL1 related Genetic Test falls under the category of Hepatology, Nephrology, and Endocrinology Disorders. It is conducted in the Genetics department of DNA Labs UAE.

Referring Doctor

A General Physician can refer patients for the LZTFL1 Gene Bardet-Biedl syndrome LZTFL1 related Genetic Test.

Pre Test Information

Before undergoing the LZTFL1 Gene Bardet-Biedl syndrome LZTFL1 related NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by LZTFL1 Gene Bardet-Biedl syndrome.

Importance of the Test

The LZTFL1 gene plays a significant role in the development of Bardet-Biedl syndrome. By identifying specific genetic variants or mutations in the LZTFL1 gene, LZTFL1 related NGS genetic testing can confirm a diagnosis of Bardet-Biedl syndrome in individuals displaying symptoms. It can also be useful for carrier testing in individuals with a family history of the syndrome, providing valuable information for genetic counseling, family planning, and potentially guiding treatment options.

Test Name LZTFL1 Gene Bardet-Biedl syndrome LZTFL1 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 LZTFL1 Gene Bardet-Biedl syndrome, LZTFL1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LZTFL1 Gene Bardet-Biedl syndrome, LZTFL1 related NGS Genetic DNA Test gene LZTFL1
Test Details

The LZTFL1 gene is associated with Bardet-Biedl syndrome (BBS), a rare genetic disorder characterized by a variety of symptoms including obesity, vision problems, kidney abnormalities, and intellectual disability.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of LZTFL1 related NGS genetic testing, it specifically focuses on sequencing the LZTFL1 gene to identify any potential genetic variants or mutations that may be associated with Bardet-Biedl syndrome.

This type of genetic testing can be helpful in confirming a diagnosis of Bardet-Biedl syndrome in individuals who exhibit symptoms of the disorder. It can also be useful for carrier testing in individuals with a family history of the syndrome, as it can identify whether they have inherited a genetic variant associated with the condition.

By identifying specific genetic variants or mutations in the LZTFL1 gene, LZTFL1 related NGS genetic testing can provide valuable information for genetic counseling, family planning, and potentially guide treatment options for individuals affected by Bardet-Biedl syndrome.

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