FKRP Gene Walker-Warburg Syndrome or Muscle-Eye-Brain Disease FKRP Related Genetic Test
Components
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 FKRP Gene Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, FKRP Related NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with FKRP Gene Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, FKRP Related
Test Details
The FKRP gene is associated with two rare genetic disorders known as Walker-Warburg Syndrome (WWS) and Muscle-Eye-Brain Disease (MEB), which are both part of a group of conditions called dystroglycanopathies. These disorders affect the development of various organs and tissues in the body, including the muscles, eyes, and brain.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, including the FKRP gene. This test can identify mutations or changes in the FKRP gene that may be responsible for causing WWS or MEB.
Genetic testing for FKRP-related disorders can be helpful in confirming a diagnosis, especially in cases where the clinical features are not clearly indicative of the condition. It can also provide information about the specific genetic mutation present, which can be important for genetic counseling and family planning.
It is important to note that genetic testing for FKRP-related disorders should be performed by a qualified healthcare professional or geneticist who specializes in genetic testing and interpretation. They will be able to provide appropriate counseling and guidance based on the test results.
| Test Name | FKRP Gene Walker-Warburg syndrome or muscle-eye-brain disease FKRP 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 FKRP Gene Walker-Warburg syndrome or muscle-eye-brain disease, FKRP related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FKRP Gene Walker-Warburg syndrome or muscle-eye-brain disease, FKRP related |
| Test Details |
The FKRP gene is associated with two rare genetic disorders known as Walker-Warburg syndrome (WWS) and muscle-eye-brain disease (MEB), which are both part of a group of conditions called dystroglycanopathies. These disorders affect the development of various organs and tissues in the body, including the muscles, eyes, and brain. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, including the FKRP gene. This test can identify mutations or changes in the FKRP gene that may be responsible for causing WWS or MEB. Genetic testing for FKRP-related disorders can be helpful in confirming a diagnosis, especially in cases where the clinical features are not clearly indicative of the condition. It can also provide information about the specific genetic mutation present, which can be important for genetic counseling and family planning. It is important to note that genetic testing for FKRP-related disorders should be performed by a qualified healthcare professional or geneticist who specializes in genetic testing and interpretation. They will be able to provide appropriate counseling and guidance based on the test results. |
