TRIM32 Gene Limb-girdle muscular dystrophy autosomal recessive type 2H Genetic Test
Components: TRIM32 Gene Limb-girdle muscular dystrophy autosomal recessive type 2H 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 TRIM32 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2H NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TRIM32 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2H.
Test Details: The TRIM32 gene is associated with limb-girdle muscular dystrophy, autosomal recessive type 2H (LGMD2H). This genetic disorder is characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders, upper arms, hips, and thighs. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of a person’s genes. In the context of LGMD2H, NGS genetic testing can be used to identify mutations or variations in the TRIM32 gene that may be responsible for the disorder. By analyzing the TRIM32 gene using NGS, healthcare professionals can provide a definitive diagnosis for LGMD2H and offer appropriate genetic counseling and management for affected individuals and their families. NGS testing can also be helpful in identifying carriers of the gene mutation, which can be important for family planning and reproductive decision-making. It is important to note that NGS genetic testing for LGMD2H should be performed by a qualified healthcare professional or genetic counselor, as they can provide appropriate pre- and post-test counseling, interpret the results accurately, and guide individuals and families in understanding the implications of the test results.
| Test Name | TRIM32 Gene Limb-girdle muscular dystrophy autosomal recessive type 2H 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 TRIM32 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2H NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TRIM32 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2H |
| Test Details | The TRIM32 gene is associated with limb-girdle muscular dystrophy, autosomal recessive type 2H (LGMD2H). This genetic disorder is characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders, upper arms, hips, and thighs. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of a person’s genes. In the context of LGMD2H, NGS genetic testing can be used to identify mutations or variations in the TRIM32 gene that may be responsible for the disorder. By analyzing the TRIM32 gene using NGS, healthcare professionals can provide a definitive diagnosis for LGMD2H and offer appropriate genetic counseling and management for affected individuals and their families. NGS testing can also be helpful in identifying carriers of the gene mutation, which can be important for family planning and reproductive decision-making. It is important to note that NGS genetic testing for LGMD2H should be performed by a qualified healthcare professional or genetic counselor, as they can provide appropriate pre- and post-test counseling, interpret the results accurately, and guide individuals and families in understanding the implications of the test results. |
