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INVS Gene Nephronophthisis Type 2 Genetic Test Cost

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

-21%

The “INVS Gene Nephronophthisis Type 2 Genetic Test” is a specialized diagnostic examination performed to detect mutations in the INVS gene, which are associated with Nephronophthisis Type 2, a rare genetic disorder. This condition is characterized by the progressive loss of kidney function, leading to end-stage renal disease. The test is particularly vital for individuals with a family history of the disease or those exhibiting symptoms, as early detection can significantly impact management and treatment options.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed for specific genetic alterations in the INVS gene. The process is highly accurate and provides crucial information for the diagnosis, prognosis, and potential treatment plans for affected individuals.

The cost of the INVS Gene Nephronophthisis Type 2 Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis and detailed reporting necessary to understand the genetic basis of the condition, offering a crucial step towards personalized medical care for patients with this rare kidney disorder.

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INVS Gene Nephronophthisis type 2 Genetic Test

Components

Test Name: INVS Gene Nephronophthisis type 2 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: Hepatology Nephrology Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for INVS Gene Nephronophthisis type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with INVS Gene Nephronophthisis type 2 NGS Genetic DNA Test gene INVS

Test Details

The INVS gene is associated with a genetic disorder called Nephronophthisis type 2 (NPHP2). Nephronophthisis is a rare genetic disorder that affects the kidneys and is characterized by the progressive loss of kidney function.

NGS (Next-Generation Sequencing) is a technology used for genetic testing that allows for the rapid and simultaneous sequencing of multiple genes. In the context of Nephronophthisis type 2, an NGS genetic test would involve sequencing the INVS gene to look for any mutations or variations that may be associated with the condition.

This type of genetic testing can help confirm a diagnosis of Nephronophthisis type 2 in individuals with symptoms suggestive of the disorder. It can also be used for carrier testing in individuals with a family history of the condition, as well as for prenatal testing in families at risk of having a child with Nephronophthisis type 2.

The results of an NGS genetic test for Nephronophthisis type 2 can provide valuable information for medical management, genetic counseling, and family planning decisions. However, it is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics.

Test Name INVS Gene Nephronophthisis type 2 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for INVS Gene Nephronophthisis type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with INVS Gene Nephronophthisis type 2 NGS Genetic DNA Test gene INVS
Test Details

The INVS gene is associated with a genetic disorder called Nephronophthisis type 2 (NPHP2). Nephronophthisis is a rare genetic disorder that affects the kidneys and is characterized by the progressive loss of kidney function.

NGS (Next-Generation Sequencing) is a technology used for genetic testing that allows for the rapid and simultaneous sequencing of multiple genes. In the context of Nephronophthisis type 2, an NGS genetic test would involve sequencing the INVS gene to look for any mutations or variations that may be associated with the condition.

This type of genetic testing can help confirm a diagnosis of Nephronophthisis type 2 in individuals with symptoms suggestive of the disorder. It can also be used for carrier testing in individuals with a family history of the condition, as well as for prenatal testing in families at risk of having a child with Nephronophthisis type 2.

The results of an NGS genetic test for Nephronophthisis type 2 can provide valuable information for medical management, genetic counseling, and family planning decisions. However, it is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics.

SKU: TEST-3725 Category:

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