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ACTN4 Gene Focal Segmental Glomerulosclerosis Type 1 Genetic Test

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

-21%

The ACTN4 Gene Focal Segmental Glomerulosclerosis Type 1 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the ACTN4 gene, which are implicated in the development of Focal Segmental Glomerulosclerosis Type 1 (FSGS Type 1). FSGS Type 1 is a rare and severe form of kidney disease that affects the glomeruli, the filtering units of the kidney, leading to significant proteinuria and potentially progressing to kidney failure.

This genetic test is crucial for individuals who have a family history of FSGS or exhibit symptoms indicative of the disease, as it allows for an accurate diagnosis, guiding treatment decisions and genetic counseling. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the ACTN4 gene known to cause FSGS Type 1.

The cost of the ACTN4 Gene Focal Segmental Glomerulosclerosis Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This investment in health can provide critical insights for affected individuals and their families, facilitating early intervention strategies and personalized management plans to mitigate the progression of the disease and improve quality of life.

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ACTN4 Gene Focal segmental glomerulosclerosis type 1 Genetic Test

Components

Price: 4400.0 AED

Sample Condition: Blood

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Hepatology Nephrology Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for ACTN4 Gene Focal segmental glomerulosclerosis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACTN4 Gene Focal segmental glomerulosclerosis type 1 NGS Genetic DNA Test gene ACTN4

Test Details

The ACTN4 gene is associated with a condition called focal segmental glomerulosclerosis (FSGS) type 1. FSGS is a kidney disorder characterized by scarring and damage to the glomeruli, which are the tiny blood vessels in the kidneys responsible for filtering waste and excess fluid from the blood.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the analysis of multiple genes simultaneously. In the context of FSGS type 1, an NGS genetic test would involve sequencing the ACTN4 gene to identify any genetic variations or mutations that may be associated with the development of the condition.

By identifying these genetic variations, healthcare providers can better understand the underlying cause of FSGS type 1 in an individual and potentially provide more targeted treatment options or genetic counseling.

Test Name ACTN4 Gene Focal segmental glomerulosclerosis type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ACTN4 Gene Focal segmental glomerulosclerosis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACTN4 Gene Focal segmental glomerulosclerosis type 1 NGS Genetic DNA Test gene ACTN4
Test Details

The ACTN4 gene is associated with a condition called focal segmental glomerulosclerosis (FSGS) type 1. FSGS is a kidney disorder characterized by scarring and damage to the glomeruli, which are the tiny blood vessels in the kidneys responsible for filtering waste and excess fluid from the blood.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the analysis of multiple genes simultaneously. In the context of FSGS type 1, an NGS genetic test would involve sequencing the ACTN4 gene to identify any genetic variations or mutations that may be associated with the development of the condition.

By identifying these genetic variations, healthcare providers can better understand the underlying cause of FSGS type 1 in an individual and potentially provide more targeted treatment options or genetic counseling.

SKU: TEST-3615 Category:

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