NIPAL4 Gene Ichthyosiform erythroderma congenital nonbullous type 1 Genetic Test
Genetic testing plays a crucial role in diagnosing and understanding various genetic conditions. One such condition is ichthyosiform erythroderma, congenital, nonbullous type 1, which is associated with the NIPAL4 gene. At DNA Labs UAE, we offer a comprehensive genetic test specifically designed to detect mutations in the NIPAL4 gene responsible for this condition.
Test Details
The NIPAL4 gene is linked to ichthyosiform erythroderma, congenital, nonbullous type 1. This rare genetic condition is characterized by the presence of dry, scaly skin resembling fish scales (ichthyosis) and redness of the skin (erythroderma) from birth. Our NGS (Next-Generation Sequencing) genetic testing utilizes advanced sequencing technology to analyze multiple genes simultaneously, enabling us to identify mutations or changes in the NIPAL4 gene.
By identifying the specific genetic mutation in the NIPAL4 gene, our NGS genetic testing provides a definitive diagnosis for individuals with ichthyosiform erythroderma, congenital, nonbullous type 1. This information is essential in understanding the underlying cause of the condition, predicting the disease’s course, and guiding treatment decisions.
It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals or genetic counselors. Our team of dermatologists and geneticists are experienced in analyzing and interpreting genetic test results, ensuring accurate diagnosis and appropriate counseling and guidance based on the results.
Test Components and Price
Our NIPAL4 Gene Ichthyosiform erythroderma congenital nonbullous type 1 Genetic Test is priced at AED 4400.0. The test can be conducted using a blood sample, extracted DNA, or a single drop of blood on an FTA Card.
Report Delivery and Method
After conducting the test, the report will be delivered within 3 to 4 weeks. We utilize NGS technology, a highly advanced sequencing method, to ensure accurate and comprehensive analysis of the NIPAL4 gene.
Test Type and Doctor
The NIPAL4 Gene Ichthyosiform erythroderma congenital nonbullous type 1 Genetic Test falls under the categories of Osteology, Dermatology, and Immunology Disorders. The test is specifically conducted by our dermatologists in the Genetics department.
Pre Test Information
Prior to conducting the NIPAL4 Gene Ichthyosiform erythroderma congenital nonbullous type 1 Genetic Test, we recommend obtaining the clinical history of the patient. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected by the condition. This information aids in better understanding the genetic inheritance pattern and assists in accurate diagnosis.
At DNA Labs UAE, we are committed to providing reliable and accurate genetic testing services. Our NIPAL4 Gene Ichthyosiform erythroderma congenital nonbullous type 1 Genetic Test offers valuable insights into the underlying cause of the condition, enabling personalized treatment and management plans. Contact us today to schedule an appointment and take a step towards understanding your genetic health.
Test Name | NIPAL4 Gene Ichthyosiform erythroderma congenital nonbullous type 1 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 | Osteology Dermatology Immunology Disorders |
Doctor | Dermatologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for NIPAL4 Gene Ichthyosiform erythroderma, congenital, nonbullous type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NIPAL4 Gene Ichthyosiform erythroderma, congenital, nonbullous type 1 NGS Genetic DNA Test gene NIPAL4 |
Test Details |
The NIPAL4 gene is associated with a rare genetic condition called ichthyosiform erythroderma, congenital, nonbullous type 1. This condition is characterized by the presence of dry, scaly skin that resembles fish scales (ichthyosis) and redness of the skin (erythroderma) from birth. 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 ichthyosiform erythroderma, NGS genetic testing can be used to identify mutations or changes in the NIPAL4 gene that are responsible for causing the condition. By identifying the specific genetic mutation in the NIPAL4 gene, NGS genetic testing can provide a definitive diagnosis for individuals with ichthyosiform erythroderma, congenital, nonbullous type 1. This information can be helpful in understanding the underlying cause of the condition, predicting the course of the disease, and guiding treatment decisions. It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and guidance based on the results. |