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SCNN1A Gene Bronchiectasis with or without elevated sweat chloride type 2 Genetic Test Cost

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

-21%

The SCNN1A gene plays a crucial role in regulating the movement of sodium in and out of cells, particularly in the lungs and sweat glands. Mutations in this gene can lead to a condition known as Bronchiectasis with or without elevated sweat chloride type 2, a rare form of lung disease characterized by chronic inflammation and infection of the bronchi, leading to their dilatation. This condition can also affect sweat chloride levels, a marker typically used for diagnosing cystic fibrosis, although it presents differently.

To diagnose this specific genetic condition, DNA Labs UAE offers a specialized genetic test targeting the SCNN1A gene. The test, priced at 4400 AED, involves analyzing the patient’s DNA to identify mutations in the SCNN1A gene that are known to cause Bronchiectasis with or without elevated sweat chloride type 2. This precise genetic testing is crucial for accurate diagnosis, guiding treatment options, and understanding the risk of passing the condition on to offspring. DNA Labs UAE utilizes advanced genetic testing techniques to ensure reliable and accurate results for patients and their families.

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SCNN1A Gene Bronchiectasis with or without elevated sweat chloride type 2 Genetic Test

At DNA Labs UAE, we offer the SCNN1A Gene Bronchiectasis with or without elevated sweat chloride type 2 Genetic Test. This test is designed to diagnose individuals with bronchiectasis and provide valuable information about the underlying genetic cause of the condition.

Test Components

  • Price: 4400.0 AED

Sample Condition

The sample condition required for this test is blood, extracted DNA, or one drop of blood on FTA card.

Report Delivery

The report will be delivered within 3 to 4 weeks.

Method

This test utilizes NGS (Next-Generation Sequencing) technology.

Test Type

This test falls under the category of metabolic disorders.

Doctor

The test can be requested by a general physician.

Test Department

This test is conducted by our Genetics department.

Pre Test Information

Prior to undergoing the SCNN1A Gene Bronchiectasis with or without elevated sweat chloride type 2 NGS Genetic DNA Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with bronchiectasis with or without elevated sweat chloride type 2.

Test Details

Bronchiectasis is a condition characterized by permanent dilation of the bronchi, leading to chronic lung infections and respiratory symptoms. The SCNN1A gene is associated with a specific type of bronchiectasis known as “bronchiectasis with or without elevated sweat chloride type 2.”

NGS (Next-Generation Sequencing) genetic testing is a comprehensive evaluation of an individual’s genetic makeup, allowing for the simultaneous analysis of multiple genes. In the case of bronchiectasis, NGS genetic testing can identify any mutations or variations in the SCNN1A gene that may be associated with the condition.

By analyzing the SCNN1A gene, NGS testing helps diagnose individuals with bronchiectasis and provides valuable information about the underlying genetic cause. This information can assist in determining appropriate treatment strategies, assessing disease severity, and offering genetic counseling for affected individuals and their families.

Test Name SCNN1A Gene Bronchiectasis with or without elevated sweat chloride 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SCNN1A Gene Bronchiectasis with or without elevated sweat chloride type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Bronchiectasis with or without elevated sweat chloride type 2
Test Details

Bronchiectasis is a condition characterized by permanent dilation of the bronchi (the airways in the lungs), leading to chronic lung infections and respiratory symptoms. The SCNN1A gene is associated with a specific type of bronchiectasis known as “bronchiectasis with or without elevated sweat chloride type 2.”

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, providing a comprehensive evaluation of an individual’s genetic makeup. In the case of bronchiectasis, NGS genetic testing can be used to identify any mutations or variations in the SCNN1A gene that may be associated with the condition.

By analyzing the SCNN1A gene, NGS testing can help diagnose individuals with bronchiectasis and provide valuable information about the underlying genetic cause of the condition. This information can be useful for determining appropriate treatment strategies, assessing disease severity, and informing genetic counseling for affected individuals and their families.

SKU: TEST-2195 Category:

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