SLC27A4 Gene Ichthyosis prematurity syndrome Genetic Test sale cost 4400 AED
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SLC27A4 Gene Ichthyosis prematurity syndrome Genetic Test Cost

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

-21%

The SLC27A4 gene plays a crucial role in the development of Ichthyosis Prematurity Syndrome (IPS), a rare genetic condition characterized by the premature birth of infants who exhibit thick, scaly skin and often face respiratory difficulties among other complications. This condition arises from mutations in the SLC27A4 gene, which is essential for the normal development of the skin’s lipid barrier.

At DNA Labs UAE, a specialized genetic test is available for accurately diagnosing Ichthyosis Prematurity Syndrome by analyzing mutations in the SLC27A4 gene. This test is particularly valuable for families with a history of IPS or for newborns presenting symptoms associated with the condition, as it aids in confirming the diagnosis and facilitating appropriate medical care and counseling.

The cost of the SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to detect the specific genetic alterations within the SLC27A4 gene that are indicative of IPS. Given the specialized nature of this test and its significance in providing a definitive diagnosis, the cost reflects the intricate processes and expertise involved in genetic testing and analysis.

In summary, the SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test offered by DNA Labs UAE is a critical tool for the diagnosis and management of this rare genetic condition, ensuring affected families receive the necessary support and medical intervention.

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SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering comprehensive genetic testing services. In this blog post, we will discuss the SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test, including its components, cost, symptoms, diagnosis, and more.

Test Components and Price

The SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test is priced at 4400.0 AED. The test requires a sample condition of either blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

The report for the SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test will be delivered within 3 to 4 weeks. The test is conducted using NGS (Next-Generation Sequencing) technology.

Test Type and Doctor

The SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. It is recommended to consult a dermatologist for this test.

Test Department and Pre Test Information

The SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test is conducted in the Genetics department. Before taking the test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the SLC27A4 Gene Ichthyosis Prematurity Syndrome.

Test Details

The SLC27A4 gene is associated with Ichthyosis Prematurity Syndrome, a rare genetic disorder characterized by skin abnormalities and premature birth. NGS genetic testing is used to analyze multiple genes simultaneously, allowing for a comprehensive assessment of genetic variations related to the condition.

For Ichthyosis Prematurity Syndrome, the NGS genetic testing focuses on sequencing the SLC27A4 gene to identify any mutations or variations that may contribute to the development of the disorder. This test helps in confirming a diagnosis, understanding the underlying genetic cause, and providing information for genetic counseling and management of the condition.

NGS genetic testing has revolutionized genetic diagnosis by enabling the analysis of large amounts of genetic data in a cost-effective and efficient manner. It has significantly improved the ability to identify genetic variations associated with various diseases, including rare genetic disorders like Ichthyosis Prematurity Syndrome.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our SLC27A4 Gene Ichthyosis Prematurity Syndrome Genetic Test can help in the diagnosis and management of this rare genetic disorder. Contact us today to schedule an appointment or learn more about our services.

Test Name SLC27A4 Gene Ichthyosis prematurity syndrome 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 SLC27A4 Gene Ichthyosis prematurity syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC27A4 Gene Ichthyosis prematurity syndrome NGS Genetic DNA Test gene SLC27A4
Test Details

The SLC27A4 gene is associated with Ichthyosis prematurity syndrome, a rare genetic disorder characterized by skin abnormalities and premature birth. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for a comprehensive assessment of genetic variations associated with a particular condition.

In the context of Ichthyosis prematurity syndrome, NGS genetic testing would involve sequencing the SLC27A4 gene to identify any mutations or variations that may be contributing to the development of the disorder. This can help in confirming a diagnosis, understanding the underlying genetic cause, and providing information for genetic counseling and management of the condition.

NGS genetic testing has revolutionized the field of genetic diagnosis, enabling the analysis of large amounts of genetic data in a cost-effective and efficient manner. It has significantly improved the ability to identify genetic variations associated with various diseases, including rare genetic disorders like Ichthyosis prematurity syndrome.

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