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NEK8 Gene Nephronophthisis Type 9 Genetic Test Cost

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

-21%

The NEK8 Gene Nephronophthisis Type 9 Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the NEK8 gene, which are associated with Nephronophthisis Type 9, a rare genetic disorder. This condition is characterized by kidney dysfunction that progressively leads to chronic kidney disease. Symptoms may include polyuria, polydipsia, anemia, and eventually end-stage renal disease. Early and accurate diagnosis through genetic testing is crucial for managing and potentially mitigating the progression of the disease.

Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, this test offers a comprehensive analysis of the NEK8 gene to identify any mutations indicative of Nephronophthisis Type 9. The cost of the test is set at 4400 AED, reflecting the intricate technologies and expert analysis involved in ensuring accurate and reliable results. Individuals who have a family history of kidney diseases or present symptoms related to Nephronophthisis are encouraged to undergo this test for early detection and to explore potential treatment options or lifestyle adjustments that may be beneficial.

Description

NEK8 Gene Nephronophthisis type 9 Genetic Test

Test Name: NEK8 Gene Nephronophthisis type 9 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 NEK8 Gene Nephronophthisis type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NEK8 Gene Nephronophthisis type 9 NGS Genetic DNA Test gene NEK8

Test Details:

The NEK8 gene is associated with a genetic disorder called nephronophthisis type 9 (NPHP9). Nephronophthisis is a rare genetic disorder that affects the kidneys and leads to kidney failure in childhood or adolescence.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of NPHP9, NGS genetic testing can be used to identify mutations or variations in the NEK8 gene that may be responsible for the development of the disorder.

NGS genetic testing for NPHP9 can help in the diagnosis of the condition, as well as provide information about the specific genetic mutation causing the disease. This information can be useful for genetic counseling, family planning, and potentially for the development of targeted treatments in the future.

It’s important to note that NGS genetic testing for NPHP9 is typically performed by specialized genetic testing laboratories and should be ordered and interpreted by healthcare professionals trained in genetics.

Test Name	NEK8 Gene Nephronophthisis type 9 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 NEK8 Gene Nephronophthisis type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NEK8 Gene Nephronophthisis type 9 NGS Genetic DNA Test gene NEK8
Test Details	The NEK8 gene is associated with a genetic disorder called nephronophthisis type 9 (NPHP9). Nephronophthisis is a rare genetic disorder that affects the kidneys and leads to kidney failure in childhood or adolescence. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of NPHP9, NGS genetic testing can be used to identify mutations or variations in the NEK8 gene that may be responsible for the development of the disorder. NGS genetic testing for NPHP9 can help in the diagnosis of the condition, as well as provide information about the specific genetic mutation causing the disease. This information can be useful for genetic counseling, family planning, and potentially for the development of targeted treatments in the future. It’s important to note that NGS genetic testing for NPHP9 is typically performed by specialized genetic testing laboratories and should be ordered and interpreted by healthcare professionals trained in genetics.