At DNA Labs UAE, we are committed to providing comprehensive genetic testing services to help diagnose and manage a variety of genetic conditions. One of the tests we offer focuses on the SCNN1A gene, which is associated with bronchiectasis with or without elevated sweat chloride, also known as type 2. This specific genetic condition can lead to significant respiratory issues, and understanding its symptoms is crucial for early diagnosis and treatment. The cost of the test is 4400 AED, and more information can be found on our website at DNA Labs UAE.
Symptoms of SCNN1A Gene Bronchiectasis
Bronchiectasis caused by mutations in the SCNN1A gene can manifest in various ways, depending on the individual. However, some common symptoms are associated with this condition, which include:
- Chronic cough: This is often the first symptom to appear and can be accompanied by the production of mucus.
- Recurrent lung infections: Individuals with this condition are more susceptible to bacterial and viral infections in the lungs.
- Shortness of breath: Difficulty breathing or shortness of breath can occur, especially during physical activity.
- Wheezing: A whistling sound when breathing may be noticeable.
- Chest pain: This can be a result of persistent coughing or lung infections.
- Fatigue: Due to the body’s increased effort to breathe and fight off infections, individuals may experience significant tiredness.
It’s important to note that symptoms can vary widely among individuals, and not everyone will experience all of these symptoms. Additionally, the severity of symptoms can also vary.
Understanding Elevated Sweat Chloride
In some cases, individuals with SCNN1A gene bronchiectasis may also exhibit elevated sweat chloride levels. This is a hallmark symptom of cystic fibrosis, but it can also occur in other genetic conditions. Elevated sweat chloride levels indicate an imbalance in the body’s ability to transport chloride ions across cell membranes, which can affect lung function and lead to additional symptoms such as:
- Saltier than normal sweat, which can lead to skin irritation or dehydration
- Increased risk of heat-related illnesses due to the body’s reduced ability to regulate temperature through sweating
Testing for elevated sweat chloride levels can be an important diagnostic tool in conjunction with genetic testing for the SCNN1A gene.
SCNN1A Gene Bronchiectasis Genetic Test at DNA Labs UAE
At DNA Labs UAE, we offer the SCNN1A gene bronchiectasis with or without elevated sweat chloride type 2 genetic test for 4400 AED. This test is designed to identify mutations in the SCNN1A gene that are associated with this condition. Early diagnosis through genetic testing can be crucial in managing symptoms and improving the quality of life for individuals with this condition.
The testing process is straightforward and involves providing a saliva or blood sample. Our state-of-the-art laboratory uses the latest technology to analyze your sample for the presence of SCNN1A gene mutations. Results are typically available within a few weeks, and our genetic counselors are available to discuss your results and what they mean for you and your family.
For more information or to schedule a test, please visit our website at DNA Labs UAE. Our team is dedicated to providing you with the highest quality genetic testing services to help you understand your genetic health.
