CRYAB Gene Myopathy Desmin Related Genetic Test
Are you experiencing muscle weakness and wasting? Do you have a family history of CRYAB gene myopathy? DNA Labs UAE offers a comprehensive genetic test to diagnose CRYAB gene myopathy, desmin-related, associated with mutations in the CRYAB gene.
Test Details
CRYAB gene myopathy, desmin-related, is a genetic disorder characterized by muscle weakness and wasting, primarily in the limbs and trunk. This condition is also linked to heart abnormalities, including cardiomyopathy. To accurately diagnose this condition, DNA Labs UAE utilizes Next-Generation Sequencing (NGS) technology.
NGS genetic testing involves sequencing the entire coding region of the CRYAB gene to identify any variations or mutations. By identifying the specific mutation in the CRYAB gene, this test provides a definitive diagnosis for individuals with CRYAB gene myopathy. This information is crucial for understanding the underlying cause of the condition, predicting disease progression, and informing treatment options and management strategies.
Test Components and Cost
The CRYAB Gene Myopathy Desmin Related Genetic Test costs AED 4400.0. The test requires either a blood sample, extracted DNA, or one drop of blood on an FTA Card. The test results will be delivered within 3 to 4 weeks.
Referring and Test Department
If you suspect you have CRYAB gene myopathy, it is recommended to consult a neurologist. The test falls under the Genetics department at DNA Labs UAE.
Pre-Test Information
Prior to the test, it is essential to provide the clinical history of the patient who is going for the CRYAB Gene Myopathy Desmin Related Genetic Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by CRYAB gene myopathy.
Test Name | CRYAB Gene Myopathy desmin related associated with mutation in the CRYAB gene Genetic Test |
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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 CRYAB Gene Myopathy, desmin related, associated with mutation in the CRYAB gene NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CRYAB Gene Myopathy, desmin related, associated with mutation in the CRYAB gene |
Test Details |
CRYAB gene myopathy, desmin-related, is a genetic disorder that is caused by mutations in the CRYAB gene. This condition is characterized by muscle weakness and wasting, particularly in the muscles of the limbs and trunk. It is also associated with heart abnormalities, such as cardiomyopathy. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to identify mutations in the CRYAB gene and other genes associated with myopathies. This test involves sequencing the entire coding region of the gene to detect any variations or mutations that may be present. By identifying the specific mutation in the CRYAB gene, NGS genetic testing can provide a definitive diagnosis for individuals with CRYAB gene myopathy. This information is important for understanding the underlying cause of the condition, predicting disease progression, and informing treatment options and management strategies. |