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FLNA Gene Otopaladigital Syndrome Type 1 Genetic Test Cost

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

-21%

The FLNA Gene Otopalatodigital Syndrome Type 1 Genetic Test is a specialized diagnostic tool designed to identify mutations in the FLNA gene, which are linked to the development of Otopalatodigital Syndrome Type 1 (OPD1). This rare genetic disorder is characterized by skeletal abnormalities, facial dysmorphisms, hearing loss, and in some cases, heart and kidney problems. The FLNA gene plays a crucial role in cell structure and signaling, and mutations in this gene can disrupt normal development and function.

The test is available at DNA Labs UAE, a leading facility in genetic testing and diagnostics. The cost of the test is 4400 AED, which reflects the comprehensive analysis involved in identifying the specific genetic mutation associated with OPD1. This test is crucial for families seeking to understand the genetic basis of the condition, potentially aiding in early intervention, management strategies, and genetic counseling. By pinpointing the exact mutation in the FLNA gene, healthcare providers can offer more personalized care and support to affected individuals and their families.

Description

FLNA Gene Otopaladigital Syndrome Type 1 Genetic Test

At DNA Labs UAE, we offer the FLNA Gene Otopaladigital Syndrome Type 1 Genetic Test. This test is designed to detect mutations in the FLNA gene, which is responsible for producing the filamin A protein. Filamin A plays a crucial role in the development and maintenance of various tissues in the body.

Otopaladigital Syndrome Type 1 is a rare genetic disorder characterized by abnormalities in the development of the ears, fingers, and toes. It is caused by mutations in the FLNA gene, which disrupt the normal function of filamin A.

Our FLNA Gene Otopaladigital Syndrome Type 1 Genetic Test utilizes NGS (Next-Generation Sequencing) technology. NGS allows for the simultaneous analysis of multiple genes or even the entire genome. In this test, we sequence the FLNA gene to identify any mutations or variations that may be present.

This genetic test is valuable for confirming a diagnosis of Otopaladigital Syndrome Type 1 in individuals with characteristic symptoms. It can also be used for carrier testing in individuals with a family history of the condition and for prenatal testing in families with a known FLNA gene mutation.

The cost of the FLNA Gene Otopaladigital Syndrome Type 1 Genetic Test is AED 4400.0. The sample condition required for testing is either blood, extracted DNA, or one drop of blood on an FTA card. The report delivery typically takes 3 to 4 weeks.

Our test is conducted in our Genetics department by experienced professionals. We recommend that patients consult with an ENT doctor, as this test falls under the category of Ear Nose Throat Disorders.

Prior to undergoing the FLNA Gene Otopaladigital Syndrome Type 1 Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session is advised to draw a pedigree chart of family members affected by the EYA1 Gene Branchiootic Syndrome Type 1 NGS Genetic DNA Test gene EYA15.

The results of this genetic test can have significant implications for medical management and treatment decisions. It can also provide valuable information about the likelihood of passing on the condition to future generations. However, it is crucial to note that genetic testing should be performed and interpreted by qualified healthcare professionals specializing in genetics.

For more information or to schedule an appointment, please contact DNA Labs UAE. We are committed to providing accurate and reliable genetic testing services.

Test Name	FLNA Gene Otopaladigital 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	Ear Nose Throat Disorders
Doctor	ENT Doctor
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA15
Test Details	FLNA gene Otopaladigital syndrome type 1 NGS genetic test is a type of genetic test that is used to detect mutations in the FLNA gene. This gene is responsible for producing a protein called filamin A, which is involved in the development and maintenance of various tissues in the body. Otopaladigital syndrome type 1 is a rare genetic disorder characterized by abnormalities in the development of the ears, fingers, and toes. It is caused by mutations in the FLNA gene, which disrupt the normal function of filamin A. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of FLNA gene Otopaladigital syndrome type 1 NGS genetic test, it involves sequencing the FLNA gene to identify any mutations or variations that may be present. This genetic test can be used to confirm a diagnosis of Otopaladigital syndrome type 1 in individuals with characteristic symptoms. It can also be used for carrier testing in individuals with a family history of the condition, as well as for prenatal testing in families with a known FLNA gene mutation. The results of the FLNA gene Otopaladigital syndrome type 1 NGS genetic test can help guide medical management and treatment decisions for individuals with the condition. It can also provide information about the likelihood of passing on the condition to future generations. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics. Genetic counseling is also recommended before and after testing to help individuals and families understand the implications of the test results.