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HYDIN Gene Primary Ciliary Dyskinesia Type 5 Genetic Test Cost

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

-21%

The HYDIN gene primary ciliary dyskinesia type 5 genetic test is a specialized diagnostic procedure designed to identify mutations in the HYDIN gene, which are associated with primary ciliary dyskinesia (PCD) type 5. PCD is a rare, inherited disorder that affects the cilia, leading to chronic respiratory tract infections, abnormal organ positioning, and fertility issues. The HYDIN gene plays a crucial role in the development and function of cilia, and mutations in this gene can disrupt ciliary motion, resulting in the symptoms of PCD.

This genetic test is crucial for early diagnosis and management of the condition, allowing for tailored treatments that can improve the quality of life for affected individuals. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in a laboratory for the presence of specific mutations in the HYDIN gene.

In the UAE, this test is available at DNA Labs UAE, a leading provider of genetic testing services in the region. The cost of the HYDIN gene primary ciliary dyskinesia type 5 genetic test at DNA Labs UAE is 4400 AED. This cost covers the collection of the sample, the genetic analysis, and a comprehensive report of the findings, which can be used by healthcare professionals to guide treatment and management decisions for patients with PCD.

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HYDIN Gene Primary Ciliary Dyskinesia Type 5 Genetic Test

Test Name: HYDIN Gene Primary Ciliary Dyskinesia Type 5 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 PTPN40

Test Details

The HYDIN gene is associated with primary ciliary dyskinesia (PCD) type 5. PCD is a rare genetic disorder that affects the structure and function of cilia, which are tiny hair-like structures that line the respiratory tract, sinuses, and other organs.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PCD, NGS can be used to identify mutations or changes in the HYDIN gene that may be causing the condition.

Testing for HYDIN gene mutations can help confirm a diagnosis of PCD type 5 and provide important information for treatment and management of the condition. It can also be used for genetic counseling and family planning purposes.

It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential risks of genetic testing before undergoing any genetic testing procedure.

Test Name HYDIN Gene Primary ciliary dyskinesia type 5 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 PTPN40
Test Details

The HYDIN gene is associated with primary ciliary dyskinesia (PCD) type 5. PCD is a rare genetic disorder that affects the structure and function of cilia, which are tiny hair-like structures that line the respiratory tract, sinuses, and other organs.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PCD, NGS can be used to identify mutations or changes in the HYDIN gene that may be causing the condition.

Testing for HYDIN gene mutations can help confirm a diagnosis of PCD type 5 and provide important information for treatment and management of the condition. It can also be used for genetic counseling and family planning purposes.

It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential risks of genetic testing before undergoing any genetic testing procedure.

SKU: TEST-2787 Category:

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