MT-TP Gene MERRF syndrome MT-TP related Genetic Test
Test Name: MT-TP Gene MERRF syndrome MT-TP related Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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 MT-TP Gene MERRF syndrome, MT-TP related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TP Gene MERRF syndrome, MT-TP related
Test Details:
MT-TP gene is a gene that is associated with MERRF (Myoclonic Epilepsy with Ragged Red Fibers) syndrome. MERRF syndrome is a rare genetic disorder that affects the mitochondria, which are responsible for producing energy in cells. This syndrome is characterized by symptoms such as myoclonic epilepsy (seizures), muscle weakness, ataxia (lack of coordination), and ragged red fibers in muscle tissue.
MT-TP related NGS Genetic Test is a genetic test that analyzes the MT-TP gene for mutations or variations that may be associated with MERRF syndrome. Next-generation sequencing (NGS) technology is used to sequence the entire MT-TP gene and identify any changes in the DNA sequence. This test can help in diagnosing MERRF syndrome and providing information about the specific genetic changes that may be causing the disorder.
The MT-TP related NGS Genetic Test is typically performed on a blood or saliva sample. The sample is sent to a laboratory where the DNA is extracted, sequenced, and analyzed. The results of the test can help healthcare professionals in confirming a diagnosis, providing genetic counseling, and guiding treatment options for individuals with MERRF syndrome.
It is important to note that genetic testing for MERRF syndrome is typically recommended for individuals who have symptoms consistent with the disorder or have a family history of the condition. Genetic testing can also be used for carrier testing or prenatal testing in families with a known MT-TP gene mutation.
Genetic testing can provide valuable information for individuals and families affected by MERRF syndrome, including a better understanding of the condition, potential risks for family members, and possible treatment options. However, it is important to consult with a healthcare professional or genetic counselor to understand the benefits, limitations, and implications of genetic testing before undergoing the test.
Test Name | MT-TP Gene MERRF syndrome MT-TP related 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 MT-TP Gene MERRF syndrome, MT-TP related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TP Gene MERRF syndrome, MT-TP related |
Test Details | MT-TP gene is a gene that is associated with MERRF (Myoclonic Epilepsy with Ragged Red Fibers) syndrome. MERRF syndrome is a rare genetic disorder that affects the mitochondria, which are responsible for producing energy in cells. This syndrome is characterized by symptoms such as myoclonic epilepsy (seizures), muscle weakness, ataxia (lack of coordination), and ragged red fibers in muscle tissue. MT-TP related NGS Genetic Test is a genetic test that analyzes the MT-TP gene for mutations or variations that may be associated with MERRF syndrome. Next-generation sequencing (NGS) technology is used to sequence the entire MT-TP gene and identify any changes in the DNA sequence. This test can help in diagnosing MERRF syndrome and providing information about the specific genetic changes that may be causing the disorder. The MT-TP related NGS Genetic Test is typically performed on a blood or saliva sample. The sample is sent to a laboratory where the DNA is extracted, sequenced, and analyzed. The results of the test can help healthcare professionals in confirming a diagnosis, providing genetic counseling, and guiding treatment options for individuals with MERRF syndrome. It is important to note that genetic testing for MERRF syndrome is typically recommended for individuals who have symptoms consistent with the disorder or have a family history of the condition. Genetic testing can also be used for carrier testing or prenatal testing in families with a known MT-TP gene mutation. Genetic testing can provide valuable information for individuals and families affected by MERRF syndrome, including a better understanding of the condition, potential risks for family members, and possible treatment options. However, it is important to consult with a healthcare professional or genetic counselor to understand the benefits, limitations, and implications of genetic testing before undergoing the test. |