TTN Gene Limb-girdle muscular dystrophy autosomal recessive type 2J Genetic Test
Are you or a loved one experiencing symptoms of limb-girdle muscular dystrophy autosomal recessive type 2J? DNA Labs UAE offers a comprehensive genetic test to diagnose this condition and provide valuable information for genetic counseling and family planning.
Test Details
The TTN gene (titin) is associated with a form of limb-girdle muscular dystrophy known as autosomal recessive type 2J (LGMD2J). This genetic disorder is characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders, hips, and limbs.
Our NGS (next-generation sequencing) genetic testing utilizes advanced sequencing technology to analyze multiple genes simultaneously. In the context of LGMD2J, NGS genetic testing can identify mutations or variations in the TTN gene that may be responsible for the development of the disorder.
Obtaining a blood or saliva sample from the affected individual is the first step in the testing process. The sample is then sent to our laboratory for analysis. Our experienced technicians use specific techniques to isolate and sequence the TTN gene, searching for any changes or mutations that may be present.
The results of the NGS genetic test can confirm a diagnosis of LGMD2J and provide crucial information for genetic counseling and family planning. Additionally, this testing can identify carriers of the gene mutation, which is useful for family members who may be at risk of passing the condition on to their children.
Test Information
- Test Name: TTN Gene Limb-girdle muscular dystrophy autosomal recessive type 2J Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Test Type: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
- Pre Test Information: Clinical History of Patient who is going for TTN Gene Limb-girdle muscular dystrophy, autosomal recessive type 2J NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TTN Gene Limb-girdle muscular dystrophy, autosomal recessive type 2J
Why Choose DNA Labs UAE?
When it comes to genetic testing, it’s crucial to seek the expertise of healthcare professionals with specialized knowledge in genetics. At DNA Labs UAE, our team of genetic counselors and medical geneticists are here to guide you through the testing process.
We understand the importance of accurate diagnosis and the impact it can have on your family’s future. Our state-of-the-art laboratory utilizes NGS technology to provide reliable and comprehensive results.
Don’t wait any longer to get the answers you need. Contact DNA Labs UAE today to schedule your TTN Gene Limb-girdle muscular dystrophy autosomal recessive type 2J Genetic Test.
| Test Name | TTN Gene Limb-girdle muscular dystrophy autosomal recessive type 2J Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for TTN Gene Limb-girdle muscular dystrophy, autosomal recessive type 2J NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TTN Gene Limb-girdle muscular dystrophy, autosomal recessive type 2J |
| Test Details |
The TTN gene (titin) is associated with a form of limb-girdle muscular dystrophy known as autosomal recessive type 2J (LGMD2J). This genetic disorder is characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders, hips, and limbs. NGS (next-generation sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of LGMD2J, NGS genetic testing can be used to identify mutations or variations in the TTN gene that may be responsible for the development of the disorder. NGS genetic testing for LGMD2J typically involves obtaining a blood or saliva sample from the affected individual, which is then sent to a laboratory for analysis. The laboratory uses specific techniques to isolate and sequence the TTN gene, looking for any changes or mutations that may be present. The results of the NGS genetic test can help confirm a diagnosis of LGMD2J and provide important information for genetic counseling and family planning. Additionally, this testing can be used to identify carriers of the gene mutation, which can be useful for family members who may be at risk of passing the condition on to their children. It’s important to note that NGS genetic testing for LGMD2J is typically ordered by a healthcare professional with expertise in genetics, such as a genetic counselor or a medical geneticist. They can provide guidance on the appropriateness of the test, the potential risks and benefits, and help interpret the results. |
