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ARHGAP31 Gene Adams-Oliver Syndrome Type 1 Genetic Test

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

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The ARHGAP31 gene plays a crucial role in the development of Adams-Oliver Syndrome Type 1, a rare genetic disorder characterized by the congenital absence of skin (aplasia cutis congenita), malformations of the skull, and limb abnormalities. DNA Labs UAE offers a specialized genetic test designed to identify mutations in the ARHGAP31 gene, which is pivotal for confirming a diagnosis of Adams-Oliver Syndrome Type 1. This targeted testing can provide essential information for affected individuals and their families regarding prognosis, potential treatments, and genetic counseling.

The test, priced at 4400 AED, involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for specific genetic alterations in the ARHGAP31 gene. Results from this test can help guide clinical management and inform about the risk of passing the condition to future generations. Conducted in a state-of-the-art facility, DNA Labs UAE ensures a high standard of accuracy and reliability for this genetic test, supporting patients and healthcare providers in making informed decisions about care and management of Adams-Oliver Syndrome Type 1.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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ARHGAP31 Gene Adams-Oliver syndrome type 1 Genetic Test

Welcome to DNA Labs UAE, where we offer the ARHGAP31 Gene Adams-Oliver syndrome type 1 Genetic Test. This test is designed to diagnose and identify mutations or variations in the ARHGAP31 gene associated with Adams-Oliver syndrome type 1 (AOS1).

Test Details

AOS1 is a rare genetic disorder characterized by the absence of skin (aplasia cutis congenita) on the scalp and limbs, as well as malformations of the fingers and toes. Our NGS (Next-Generation Sequencing) genetic testing method allows us to analyze multiple genes simultaneously, including the ARHGAP31 gene.

By sequencing the entire coding region of the ARHGAP31 gene, our NGS testing can provide a comprehensive analysis of the gene’s sequence and identify any potential pathogenic variants. This information is crucial in confirming a diagnosis of AOS1 and providing genetic counseling to affected individuals and their families.

Test Components

  • Test Name: ARHGAP31 Gene Adams-Oliver syndrome type 1 Genetic Test
  • 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

Before undergoing the ARHGAP31 Gene Adams-Oliver syndrome type 1 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by ARHGAP31 Gene Adams-Oliver syndrome type 1 NGS Genetic DNA Test gene ARHGAP31.

Genetic Testing Process

It is crucial to have genetic testing for AOS1 performed by a qualified healthcare professional or geneticist who specializes in genetic disorders. They will guide individuals through the testing process, interpret the results, and provide appropriate counseling and management recommendations.

Our ARHGAP31 Gene Adams-Oliver syndrome type 1 Genetic Test is a valuable tool in diagnosing and managing AOS1. With our NGS technology and expertise in genetics, we aim to provide accurate and comprehensive genetic testing services to individuals and families.

Test Name ARHGAP31 Gene Adams-Oliver syndrome 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 ARHGAP31 Gene Adams-Oliver syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ARHGAP31 Gene Adams-Oliver syndrome type 1 NGS Genetic DNA Test gene ARHGAP31
Test Details

The ARHGAP31 gene is associated with Adams-Oliver syndrome type 1 (AOS1). AOS1 is a rare genetic disorder characterized by the absence of skin (aplasia cutis congenita) on the scalp and limbs, as well as malformations of the fingers and toes.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of AOS1, NGS genetic testing can be used to identify mutations or variations in the ARHGAP31 gene that may be causing the disorder.

By sequencing the entire coding region of the ARHGAP31 gene, NGS testing can provide a comprehensive analysis of the gene’s sequence and identify any potential pathogenic variants. This information can help in confirming a diagnosis of AOS1 and providing genetic counseling to affected individuals and their families.

It is important to note that genetic testing for AOS1 should be performed by a qualified healthcare professional or geneticist who specializes in genetic disorders. They can guide individuals through the testing process, interpret the results, and provide appropriate counseling and management recommendations.

SKU: TEST-2810 Category:

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