FBLN5 Gene Cutis Laxa Type 2 Autosomal Dominant NGS Genetic DNA Test
Introduction
The FBLN5 Gene Cutis Laxa Type 2 Autosomal Dominant NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the FBLN5 gene, which are responsible for cutis laxa, a rare connective tissue disorder. This test is crucial for patients displaying symptoms of cutis laxa, as it can provide definitive answers and guide treatment options.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the FBLN5 gene. It detects specific mutations that can lead to the development of cutis laxa type 2, allowing for an accurate diagnosis and better understanding of the condition.
Who Should Consider This Test
Individuals who exhibit symptoms such as skin laxity, joint hypermobility, and other related features should consider this test. Additionally, those with a family history of cutis laxa or related genetic disorders may benefit from undergoing testing.
Benefits of Taking the Test
- Provides a definitive diagnosis for patients with symptoms of cutis laxa.
- Helps in understanding the genetic basis of the condition.
- Guides management and treatment options based on genetic findings.
- Enables family planning and genetic counseling for affected families.
Understanding Your Results
Results from the FBLN5 Gene Cutis Laxa Type 2 Autosomal Dominant NGS Genetic DNA Test will indicate whether any mutations were detected in the FBLN5 gene. A genetic counselor will assist in interpreting these results and discussing potential implications for you and your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FBLN5 Gene Cutis Laxa Type 2 Autosomal Dominant NGS Genetic DNA Test | KSh 40,000 | KSh 56,000 |
Additional Information
The turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or even one drop of blood on an FTA card. Prior to testing, a clinical history of the patient is necessary, along with a genetic counseling session to draw a pedigree chart of family members affected by the FBLN5 gene.
We have branches across Kenya, and we also offer home sample collection services for your convenience. To book the FBLN5 Gene Cutis Laxa Type 2 Autosomal Dominant NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
