CACNA1D Gene Sinoatrial Node Dysfunction and Deafness Genetic Test sale cost 4400 AED
DNAI2 Gene Primary Ciliary Dyskinesia Type 9 Genetic Test sale cost 4400 AED DNAI2 Gene Primary Ciliary Dyskinesia Type 9 Genetic Test 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
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CACNA1D Gene Sinoatrial Node Dysfunction and Deafness Genetic Test

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

-21%

The “CACNA1D Gene Sinoatrial Node Dysfunction and Deafness Genetic Test” is a specialized diagnostic examination offered at DNA Labs UAE, designed to identify mutations in the CACNA1D gene. These mutations are known to be associated with a rare condition that affects both the heart and hearing, leading to sinoatrial node dysfunction and deafness. The sinoatrial node is crucial for heart rhythm regulation, and its dysfunction can lead to arrhythmias and other cardiac issues. Concurrently, mutations in the CACNA1D gene can also impact auditory function, leading to various degrees of hearing loss.

This genetic test is crucial for individuals who exhibit symptoms of either condition or have a family history of sinoatrial node dysfunction or deafness, as it can provide definitive genetic evidence of the mutation. Early detection through this test allows for timely management and treatment of the conditions, potentially improving the quality of life and health outcomes for affected individuals.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to analyze genetic information accurately. Results from this test can guide healthcare professionals in creating a personalized treatment plan for patients, taking into account their specific genetic makeup and the potential risks associated with these genetic mutations.

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CACNA1D Gene Sinoatrial Node Dysfunction and Deafness Genetic Test

Test Name: CACNA1D Gene Sinoatrial Node Dysfunction and Deafness 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 PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN41

Test Details

The CACNA1D gene is associated with both sinoatrial node dysfunction and deafness. Sinoatrial node dysfunction refers to abnormalities in the heart’s natural pacemaker, which can lead to irregular heartbeats and other cardiac issues. Deafness, on the other hand, refers to a partial or complete loss of hearing.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify any genetic variations or mutations that may be associated with a particular condition. In the case of the CACNA1D gene, NGS genetic testing can be used to identify any mutations or variations in this gene that may be causing sinoatrial node dysfunction and/or deafness.

By analyzing the CACNA1D gene through NGS genetic testing, healthcare professionals can determine if there are any specific genetic variations or mutations that may be contributing to the development of these conditions. This information can help in diagnosing and managing the conditions, as well as providing genetic counseling and guidance for affected individuals and their families.

Test Name CACNA1D Gene Sinoatrial node dysfunction and deafness 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 PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN41
Test Details

The CACNA1D gene is associated with both sinoatrial node dysfunction and deafness. Sinoatrial node dysfunction refers to abnormalities in the heart’s natural pacemaker, which can lead to irregular heartbeats and other cardiac issues. Deafness, on the other hand, refers to a partial or complete loss of hearing.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify any genetic variations or mutations that may be associated with a particular condition. In the case of the CACNA1D gene, NGS genetic testing can be used to identify any mutations or variations in this gene that may be causing sinoatrial node dysfunction and/or deafness.

By analyzing the CACNA1D gene through NGS genetic testing, healthcare professionals can determine if there are any specific genetic variations or mutations that may be contributing to the development of these conditions. This information can help in diagnosing and managing the conditions, as well as providing genetic counseling and guidance for affected individuals and their families.

SKU: TEST-2794 Category:

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