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FLNA Gene Otopaladigital Syndrome Type 2 Genetic Test Cost

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

-21%

The FLNA Gene Otopalatodigital Syndrome Type 2 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the FLNA gene, which are linked to Otopalatodigital Syndrome Type 2 (OPD2). OPD2 is a rare genetic disorder characterized by skeletal abnormalities, distinctive facial features, and possible intellectual disabilities. The FLNA gene plays a crucial role in cell structure and movement, and mutations in this gene can disrupt normal skeletal development.

This test is crucial for individuals showing symptoms of OPD2 or those with a family history of the condition, as it provides a definitive diagnosis by identifying specific genetic alterations in the FLNA gene. The procedure involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations associated with the syndrome.

The cost of the FLNA Gene Otopalatodigital Syndrome Type 2 Genetic Test at DNA Labs UAE is 4400 AED. Given the specialized nature of this test and its importance in the accurate diagnosis and management of OPD2, the investment is invaluable for affected families. Early diagnosis through genetic testing can lead to better management of the syndrome’s symptoms and improved quality of life for those affected.

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FLNA Gene Otopaladigital Syndrome Type 2 Genetic Test

Test Name: FLNA Gene Otopaladigital Syndrome Type 2 Genetic Test

Components: FLNA gene analysis

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: Ear Nose Throat Disorders

Doctor: ENT Doctor

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A17

Test Details

The FLNA Gene Otopaladigital Syndrome Type 2 NGS Genetic Test is a genetic test that analyzes the FLNA gene for mutations associated with Otopaladigital Syndrome Type 2. This rare genetic disorder is characterized by skeletal abnormalities, hearing loss, and intellectual disability.

The FLNA gene provides instructions for making the filamin A protein, which is essential for the development and maintenance of various tissues in the body, including the skeleton and brain.

The NGS (Next-Generation Sequencing) genetic test uses advanced sequencing technology to analyze the FLNA gene for mutations. By detecting specific changes in the gene’s DNA sequence, this test can help confirm a diagnosis of Otopaladigital Syndrome Type 2.

Additionally, the test provides valuable information for genetic counseling and management of the disorder. It is typically ordered by healthcare professionals such as geneticists or genetic counselors, who will interpret the results and provide appropriate recommendations based on the individual’s specific situation.

It is important to note that genetic testing can have implications for the individual and their family members. Therefore, it is crucial to have a thorough understanding of the test and its potential outcomes before proceeding.

Test Name FLNA Gene Otopaladigital syndrome type 2 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 Ear Nose Throat Disorders
Doctor ENT Doctor
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A17
Test Details

FLNA Gene Otopaladigital syndrome type 2 NGS Genetic Test is a genetic test that analyzes the FLNA gene for mutations associated with Otopaladigital syndrome type 2. Otopaladigital syndrome type 2 is a rare genetic disorder characterized by skeletal abnormalities, hearing loss, and intellectual disability. The FLNA gene provides instructions for making the filamin A protein, which plays a role in the development and maintenance of various tissues in the body, including the skeleton and brain.

The NGS (Next-Generation Sequencing) genetic test uses advanced sequencing technology to analyze the FLNA gene for mutations. This test can identify specific changes in the gene’s DNA sequence that may be responsible for causing Otopaladigital syndrome type 2. By detecting these mutations, the test can help confirm a diagnosis of the condition and provide valuable information for genetic counseling and management of the disorder.

It is important to note that this test is typically ordered by a healthcare professional, such as a geneticist or genetic counselor, who will interpret the results and provide appropriate recommendations based on the individual’s specific situation. Genetic testing can have implications for the individual and their family members, so it is important to have a thorough understanding of the test and its potential outcomes before proceeding.

SKU: TEST-2763 Category:

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