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FBLN5 Gene Cutis Laxa Type 1A Autosomal Recessive Genetic Test Cost

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

-21%

The FBLN5 Gene Cutis Laxa Type 1A Autosomal Recessive Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the FBLN5 gene, which are known to cause Cutis Laxa Type 1A. Cutis Laxa is a rare genetic disorder characterized by severely loose and sagging skin, alongside other possible systemic involvement affecting lungs, arteries, and the gastrointestinal system. Type 1A is inherited in an autosomal recessive pattern, meaning an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the disorder.

The test is crucial for early diagnosis, enabling appropriate management and genetic counseling for affected families. It involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of specific mutations in the FBLN5 gene that are indicative of Cutis Laxa Type 1A.

Priced at 4400 AED, this genetic test is an important resource for individuals with a family history of Cutis Laxa or those showing symptoms of the disorder, providing them with critical information for managing their health and making informed decisions about their future and that of their potential offspring. DNA Labs UAE, by offering this test, plays a vital role in the early detection and management of this rare genetic condition.

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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FBLN5 Gene Cutis laxa type 1A autosomal recessive Genetic Test

Welcome to DNA Labs UAE, where we offer the FBLN5 Gene Cutis laxa type 1A autosomal recessive Genetic Test. In this blog post, we will provide detailed information about this test, including its cost, symptoms, diagnosis, and more.

Test Details

The FBLN5 gene is associated with Cutis laxa type 1A, which is an autosomal recessive disorder. Our NGS (Next-Generation Sequencing) genetic testing method allows us to analyze the DNA sequence of the FBLN5 gene and identify any mutations or variations that may be present. This test is highly accurate and can help confirm a diagnosis of Cutis laxa type 1A. It also provides valuable information about the specific genetic variant causing the condition.

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

Prior to undergoing the FBLN5 Gene Cutis laxa type 1A autosomal recessive Genetic 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 with the FBLN5 Gene Cutis laxa type 1A autosomal recessive NGS Genetic DNA Test gene FBLN5.

Conclusion

If you or a family member is suspected to have Cutis laxa type 1A, our FBLN5 Gene Cutis laxa type 1A autosomal recessive Genetic Test can provide valuable insights. With our advanced NGS technology, we can accurately diagnose this genetic disorder and provide information about the specific genetic variant causing it. Don’t hesitate to contact DNA Labs UAE for more information or to schedule an appointment for this test.

Test Name FBLN5 Gene Cutis laxa type 1A autosomal recessive 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 FBLN5 Gene Cutis laxa type 1A, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBLN5 Gene Cutis laxa type 1A, autosomal recessive NGS Genetic DNA Test gene FBLN5
Test Details

FBLN5 gene is associated with Cutis laxa type 1A, which is an autosomal recessive disorder. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the FBLN5 gene and identify any mutations or variations that may be present. This test can help in confirming a diagnosis of Cutis laxa type 1A and provide information about the specific genetic variant causing the condition. It can also be used for carrier testing in individuals with a family history of Cutis laxa type 1A.