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FKTN Gene Walker-Warburg Syndrome Genetic Test Cost

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

-21%

The FKTN Gene Walker-Warburg Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the FKTN gene, which are known to cause Walker-Warburg Syndrome (WWS). WWS is a rare genetic disorder characterized by severe brain malformations, muscle weakness, and eye abnormalities. Early and accurate diagnosis through this genetic test allows for better understanding of the condition, guiding treatment and management decisions for affected individuals.

Priced at 4400 AED, the test involves collecting a DNA sample, typically through a blood draw, and analyzing the genetic material for specific mutations in the FKTN gene. This gene plays a crucial role in the development and maintenance of muscle and brain tissue, and mutations can lead to the symptoms associated with WWS.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the FKTN Gene Walker-Warburg Syndrome Genetic Test provides families with critical information regarding the genetic makeup and potential health challenges their loved ones may face, enabling informed healthcare decisions and support for managing the condition.

Description

FKTN Gene Walker-Warburg syndrome Genetic Test

Components: FKTN Gene Walker-Warburg syndrome 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 FKTN Gene Walker-Warburg syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FKTN Gene Walker-Warburg syndrome.

Test Details:

The FKTN gene is associated with a rare genetic disorder called Walker-Warburg syndrome (WWS). WWS is a severe form of congenital muscular dystrophy that affects the development of the brain and other organs. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously.

In the case of Walker-Warburg syndrome, NGS genetic testing can be used to analyze the FKTN gene for any potential disease-causing mutations or variations. This type of genetic testing can help in diagnosing individuals with Walker-Warburg syndrome and can also be used for carrier testing in individuals with a family history of the disorder.

Identifying disease-causing mutations in the FKTN gene can provide valuable information for genetic counseling, family planning, and potential treatment options.

Test Name	FKTN Gene Walker-Warburg syndrome 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 FKTN Gene Walker-Warburg syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FKTN Gene Walker-Warburg syndrome
Test Details	The FKTN gene is associated with a rare genetic disorder called Walker-Warburg syndrome (WWS). WWS is a severe form of congenital muscular dystrophy that affects the development of the brain and other organs. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Walker-Warburg syndrome, NGS genetic testing can be used to analyze the FKTN gene for any potential disease-causing mutations or variations. This type of genetic testing can help in diagnosing individuals with Walker-Warburg syndrome and can also be used for carrier testing in individuals with a family history of the disorder. Identifying disease-causing mutations in the FKTN gene can provide valuable information for genetic counseling, family planning, and potential treatment options.