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FBLN5 Gene Cutis laxa type 2, autosomal dominant NGS Genetic DNA Test Cost 20000 Rs
FBLN5 Gene Cutis laxa type 2, autosomal dominant NGS Genetic DNA Test Details
FBLN5 Gene Cutis Laxa Type 2: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost
Are you or someone you know experiencing symptoms of Cutis Laxa Type 2? It may be caused by a genetic mutation in the FBLN5 gene, which affects the production of elastin in the body. This condition is autosomal dominant, meaning it can be passed down through generations. The good news is that there is now a Next-Generation Sequencing (NGS) Genetic DNA Test available to diagnose this condition.
Symptoms of Cutis Laxa Type 2
The symptoms of Cutis Laxa Type 2 can vary from person to person, but typically include:
- Loose, saggy skin
- Wrinkles
- Poor wound healing
- Joint hypermobility
- Respiratory problems
- Gastrointestinal problems
- Developmental delays
- Intellectual disability
Diagnosis of Cutis Laxa Type 2
If you or a loved one are experiencing these symptoms, it is important to see a doctor or genetic counselor for a diagnosis. A physical exam can reveal some of the characteristic signs of Cutis Laxa Type 2, but a definitive diagnosis can only be made through genetic testing.
NGS Genetic DNA Test for Cutis Laxa Type 2
The NGS Genetic DNA Test for Cutis Laxa Type 2 is a non-invasive test that can detect mutations in the FBLN5 gene. This test is highly accurate and can provide a diagnosis in a matter of weeks.
The cost of the NGS Genetic DNA Test for Cutis Laxa Type 2 at DNA Labs India is INR 20,000. This cost includes the genetic counseling and interpretation of results.
Conclusion
Cutis Laxa Type 2 is a rare genetic condition that can have a significant impact on a person's quality of life. If you or a loved one are experiencing symptoms of this condition, it is important to seek a diagnosis through genetic testing. The NGS Genetic DNA Test for Cutis Laxa Type 2 offered by DNA Labs India is a reliable and affordable option for those seeking answers.
Don't wait, get tested and start your journey towards a better life today!
Contact DNA Labs India for more information on this test and other genetic testing options.
Cutis laxa type 2, autosomal dominant (ADCL2) is a rare genetic disorder characterized by loose and sagging skin, as well as other connective tissue abnormalities. Mutations in the FBLN5 gene have been associated with this condition.