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DYX1C1 Gene Primary Ciliary Dyskinesia Type 25 Genetic Test Cost

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

-21%

The DYX1C1 Gene Primary Ciliary Dyskinesia Type 25 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the DYX1C1 gene that are associated with Primary Ciliary Dyskinesia (PCD) Type 25. PCD is a rare genetic disorder characterized by chronic respiratory tract infections, abnormal organ positioning, and infertility due to defects in the structure and function of cilia. The DYX1C1 gene plays a crucial role in the development and function of cilia, and mutations in this gene can lead to the symptoms observed in PCD Type 25.

This genetic test is essential for the accurate diagnosis of PCD Type 25, enabling healthcare providers to tailor treatments and management strategies to the specific needs of the patient. Early diagnosis and intervention can significantly improve the quality of life for individuals with this condition. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the DYX1C1 gene.

At DNA Labs UAE, the cost of the DYX1C1 Gene Primary Ciliary Dyskinesia Type 25 Genetic Test is 4400 AED. The test is conducted with the utmost care and precision, ensuring reliable results for patients and their families. With advanced genetic testing capabilities, DNA Labs UAE is at the forefront of providing critical diagnostic services that contribute to the effective management of genetic disorders like Primary Ciliary Dyskinesia.

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DYX1C1 Gene Primary Ciliary Dyskinesia Type 25 Genetic Test

Welcome to DNA Labs UAE, a leading genetic laboratory in the UAE. We offer a comprehensive range of genetic tests, including the DYX1C1 Gene Primary Ciliary Dyskinesia Type 25 Genetic Test. In this blog post, we will discuss the test details, symptoms, diagnosis, and cost of this genetic test.

Test Name: DYX1C1 Gene Primary Ciliary Dyskinesia Type 25 Genetic Test

Components: This test includes the analysis of the DYX1C1 gene.

Price: AED 4400.0

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: It is recommended to provide the clinical history of the patient who is going for the CATSPER2 Gene Deafness and male infertility test. A genetic counseling session is also advised to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility.

Test Details

The DYX1C1 gene is associated with primary ciliary dyskinesia type 25 (PCD25), a rare genetic disorder that affects the function of cilia in the respiratory tract. This disorder can lead to chronic respiratory infections and other respiratory problems. By performing NGS genetic testing, we can analyze multiple genes simultaneously, including the DYX1C1 gene, to identify any mutations or variations that may be responsible for the development of PCD25.

NGS genetic testing, also known as Next-Generation Sequencing, utilizes advanced sequencing technology to provide a more accurate diagnosis of genetic disorders. By analyzing the DYX1C1 gene through NGS, our healthcare professionals can offer personalized treatment options based on the specific genetic variations found in an individual’s genes.

It is important to note that genetic testing for PCD25 or any other genetic disorder should always be done under the guidance of a healthcare professional, such as a genetic counselor or geneticist. These professionals can help interpret the test results and provide appropriate counseling and support.

If you are interested in the DYX1C1 Gene Primary Ciliary Dyskinesia Type 25 Genetic Test or any other genetic tests, please contact DNA Labs UAE. Our team of experts is dedicated to providing accurate and reliable genetic testing services.

Test Name DYX1C1 Gene Primary ciliary dyskinesia type 25 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 CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER18
Test Details

The DYX1C1 gene is associated with primary ciliary dyskinesia type 25 (PCD25), a rare genetic disorder that affects the function of cilia in the respiratory tract, resulting in chronic respiratory infections and other respiratory problems.

NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PCD25, NGS genetic testing can be used to identify mutations or variations in the DYX1C1 gene that may be responsible for the development of the disorder.

By analyzing the DYX1C1 gene through NGS, healthcare professionals can provide a more accurate diagnosis of PCD25 and offer personalized treatment options based on the specific genetic variations found in an individual’s genes.

It is important to note that genetic testing for PCD25 or any other genetic disorder should be done under the guidance of a healthcare professional, such as a genetic counselor or geneticist, who can help interpret the results and provide appropriate counseling and support.