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NIPAL4 Gene Ichthyosiform erythroderma congenital nonbullous type 1 Genetic Test Cost

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

-21%

The NIPAL4 Gene Ichthyosiform Erythroderma Congenital Nonbullous Type 1 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the NIPAL4 gene. These mutations are responsible for causing Ichthyosiform Erythroderma Congenital Nonbullous Type 1, a rare genetic skin disorder characterized by red, inflamed, and scaly skin present from birth. The condition is part of a group known as autosomal recessive congenital ichthyoses (ARCI), which affects the skin’s ability to retain moisture and protect against infections.

This genetic test is crucial for accurate diagnosis and guiding treatment strategies, offering insights into the genetic underpinnings of the condition. The procedure involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the NIPAL4 gene.

The cost of the test at DNA Labs UAE is 4400 AED, reflecting the specialized nature of the test and the comprehensive analysis it entails. This investment is vital for affected individuals and their families seeking a definitive diagnosis and understanding of the condition, potentially leading to more personalized and effective management strategies.

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  • This test is not intended for medical diagnosis or treatment
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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.

SKU: TEST-3046 Category:

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