Ichthyosis lamellar type 3 is a rare genetic condition that significantly impacts the skin, causing it to become dry, scaly, and thickened. This condition is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected. The CYP4F22 gene has been identified as one of the genes responsible for this condition. Understanding the symptoms associated with mutations in the CYP4F22 gene is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for those who suspect they may be carriers or affected by Ichthyosis lamellar type 3.
Symptoms of CYP4F22 Gene Ichthyosis Lamellar Type 3
Individuals with mutations in the CYP4F22 gene may exhibit a range of symptoms, primarily affecting the skin. These symptoms can vary in severity and may include:
- Scaly Skin: The hallmark symptom of Ichthyosis lamellar type 3 is the presence of large, dark scales that cover the body. These scales can cause discomfort and may lead to cracking and peeling.
- Dry Skin: Affected individuals often have extremely dry skin, which can lead to itching and irritation.
- Ectropion: Ectropion, or the outward turning of the eyelid, is a common symptom that can lead to further complications, such as dry eyes and vision problems.
- Increased Risk of Infections: The skin’s barrier function is compromised in individuals with Ichthyosis lamellar type 3, leading to an increased risk of skin infections.
- Difficulty with Temperature Regulation: The thickened skin can interfere with sweat production and evaporation, making it challenging for affected individuals to regulate their body temperature.
It is important to note that the severity of symptoms can vary widely among individuals with the same genetic mutation. Early diagnosis and intervention can help manage symptoms and improve the quality of life for those affected.
Genetic Testing for CYP4F22 Gene Ichthyosis Lamellar Type 3
DNA Labs UAE offers a genetic test specifically designed to identify mutations in the CYP4F22 gene associated with Ichthyosis lamellar type 3. This test is an invaluable tool for families with a history of the condition, individuals showing symptoms, or couples planning to have children who want to understand their genetic risk. The test involves a simple sample collection process, after which the sample is analyzed for the presence of mutations in the CYP4F22 gene.
The cost of the genetic test for the CYP4F22 gene at DNA Labs UAE is 3200 AED. This price includes the cost of the sample collection kit, laboratory analysis, and a comprehensive report of the findings. The report will provide detailed information about the presence of any mutations in the CYP4F22 gene and guidance on the next steps for individuals and families.
For more information about the CYP4F22 gene Ichthyosis lamellar type 3 genetic test and to schedule your test, please visit DNA Labs UAE.
Understanding your genetic makeup can empower you with the knowledge to make informed decisions about your health and the health of your family. Early detection and diagnosis of genetic conditions like Ichthyosis lamellar type 3 can lead to better management strategies and a higher quality of life. DNA Labs UAE is committed to providing accurate, confidential, and timely genetic testing services to help you and your loved ones live healthier lives.
