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ALOXE3 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 ALOXE3 gene plays a significant role in the development of a rare skin disorder known as Congenital Nonbullous Ichthyosiform Erythroderma (CIE) Type 1. This genetic condition is characterized by widespread redness of the skin and scaling that appears shortly after birth. The ALOXE3 gene is crucial for the proper formation of the lipid barrier of the skin, which is why mutations in this gene can lead to the symptoms observed in affected individuals.

DNA Labs UAE offers a specialized genetic test to identify mutations in the ALOXE3 gene, which can confirm a diagnosis of CIE Type 1. This test is particularly important for families with a history of the condition or for new parents noticing the symptoms in their newborn. Early diagnosis can help in managing the symptoms more effectively and in understanding the condition better.

The cost of the ALOXE3 Gene Ichthyosiform Erythroderma Congenital Nonbullous Type 1 Genetic Test at DNA Labs UAE is 4400 AED. The test is conducted using a sample of the patient’s blood or saliva, and it involves analyzing the DNA for specific mutations in the ALOXE3 gene that are known to cause the disorder. Results from the test can provide crucial information for the affected individuals and their families regarding the management of the condition and the risk of passing it on to future generations.

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ALOXE3 Gene Ichthyosiform erythroderma congenital nonbullous type 1 Genetic Test

Test Name: ALOXE3 Gene Ichthyosiform erythroderma congenital nonbullous type 1 Genetic Test

Components: ALOXE3 gene analysis

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 ALOXE3 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 ALOXE3 Gene Ichthyosiform erythroderma, congenital, nonbullous type 1 NGS Genetic DNA Test gene ALOXE3

Test Details: The ALOXE3 gene is associated with a genetic condition called Ichthyosiform erythroderma, congenital, nonbullous type 1. This condition is characterized by the presence of dry, scaly skin that resembles fish scales. It is a rare inherited disorder that affects the skin’s ability to function properly. NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that allows for the analysis of multiple genes simultaneously. In the context of Ichthyosiform erythroderma, congenital, nonbullous type 1, an NGS Genetic Test can be used to identify mutations or variations in the ALOXE3 gene. By analyzing the ALOXE3 gene, this test can provide valuable information about the specific genetic changes that may be causing the condition. This can help in confirming a diagnosis, understanding the inheritance pattern, and providing genetic counseling to affected individuals and their families. It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor, who can interpret the results and provide appropriate recommendations and support.

Test Name ALOXE3 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 ALOXE3 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 ALOXE3 Gene Ichthyosiform erythroderma, congenital, nonbullous type 1 NGS Genetic DNA Test gene ALOXE3
Test Details

The ALOXE3 gene is associated with a genetic condition called Ichthyosiform erythroderma, congenital, nonbullous type 1. This condition is characterized by the presence of dry, scaly skin that resembles fish scales. It is a rare inherited disorder that affects the skin’s ability to function properly.

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that allows for the analysis of multiple genes simultaneously. In the context of Ichthyosiform erythroderma, congenital, nonbullous type 1, an NGS Genetic Test can be used to identify mutations or variations in the ALOXE3 gene.

By analyzing the ALOXE3 gene, this test can provide valuable information about the specific genetic changes that may be causing the condition. This can help in confirming a diagnosis, understanding the inheritance pattern, and providing genetic counseling to affected individuals and their families.

It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor, who can interpret the results and provide appropriate recommendations and support.