DNAJB6 Gene Limb-girdle muscular dystrophy autosomal dominant type 1E Genetic Test
Components: DNAJB6 Gene Limb-girdle muscular dystrophy autosomal dominant type 1E 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: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for DNAJB6 Gene Limb-girdle muscular dystrophy, autosomal dominant type 1E NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DNAJB6 Gene Limb-girdle muscular dystrophy, autosomal dominant type 1E
Test Details
The DNAJB6 gene is associated with limb-girdle muscular dystrophy, autosomal dominant type 1E (LGMD1E). This is a genetic disorder characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders and hips (limb-girdle muscles). It is inherited in an autosomal dominant pattern, meaning that an affected individual has a 50% chance of passing the gene mutation to each of their children.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously to identify mutations or variations in an individual’s DNA. In the context of LGMD1E, NGS genetic testing can be used to identify mutations in the DNAJB6 gene, which can confirm a diagnosis of LGMD1E in an affected individual or identify individuals who carry the gene mutation but may not yet show symptoms.
NGS genetic testing can be helpful in diagnosing genetic disorders, providing information about disease progression and prognosis, and guiding treatment decisions. It can also be used for carrier testing, allowing individuals to determine if they carry a gene mutation that could be passed on to their children.
It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support before and after testing.
| Test Name | DNAJB6 Gene Limb-girdle muscular dystrophy autosomal dominant type 1E 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 DNAJB6 Gene Limb-girdle muscular dystrophy, autosomal dominant type 1E NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DNAJB6 Gene Limb-girdle muscular dystrophy, autosomal dominant type 1E |
| Test Details | The DNAJB6 gene is associated with limb-girdle muscular dystrophy, autosomal dominant type 1E (LGMD1E). This is a genetic disorder characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders and hips (limb-girdle muscles). It is inherited in an autosomal dominant pattern, meaning that an affected individual has a 50% chance of passing the gene mutation to each of their children. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously to identify mutations or variations in an individual’s DNA. In the context of LGMD1E, NGS genetic testing can be used to identify mutations in the DNAJB6 gene, which can confirm a diagnosis of LGMD1E in an affected individual or identify individuals who carry the gene mutation but may not yet show symptoms. NGS genetic testing can be helpful in diagnosing genetic disorders, providing information about disease progression and prognosis, and guiding treatment decisions. It can also be used for carrier testing, allowing individuals to determine if they carry a gene mutation that could be passed on to their children. It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support before and after testing. |
