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FKRP Gene Walker-Warburg Syndrome or Muscle-Eye-Brain Disease FKRP Related Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The FKRP gene (Fukutin-Related Protein gene) plays a critical role in the proper development and maintenance of muscle tissue, the brain, and the eyes. Mutations in the FKRP gene can lead to severe congenital disorders such as Walker-Warburg Syndrome (WWS) and Muscle-Eye-Brain (MEB) Disease. These conditions are characterized by muscle weakness, structural brain defects, and eye abnormalities. They are part of a group of diseases known as congenital muscular dystrophies.

To diagnose these conditions and understand the genetic basis in affected individuals, genetic testing focusing on the FKRP gene is essential. DNA Labs UAE offers a comprehensive FKRP Related Genetic Test, which is a vital tool in diagnosing conditions like Walker-Warburg Syndrome or Muscle-Eye-Brain Disease. This test is particularly crucial for families with a history of these disorders, as it can provide valuable information for disease management and genetic counseling.

The test is conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities. The cost of the FKRP Related Genetic Test is 4400 AED. This investment can be invaluable for affected families, offering insights into the genetic mutations responsible for these conditions and facilitating informed decisions regarding care and treatment.

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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.

SKU: TEST-2109 Category:

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