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WDR19 Gene Nephronophthisis Type 13 Genetic Test Cost

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

-21%

The WDR19 gene nephronophthisis type 13 genetic test is a specialized diagnostic tool designed to identify mutations in the WDR19 gene, which are implicated in causing nephronophthisis type 13, a rare genetic disorder. Nephronophthisis is a form of kidney disease that primarily affects children and young adults, leading to chronic kidney failure. It is characterized by symptoms such as polyuria, polydipsia, anemia, and progression to end-stage renal disease.

This genetic test is crucial for early detection and management of the condition, allowing healthcare providers to tailor treatment plans according to the specific genetic mutation present. The test involves analyzing the patient’s DNA to look for mutations in the WDR19 gene that are known to cause the disease. Early diagnosis through genetic testing can significantly impact the management of nephronophthisis, enabling interventions that can delay the progression of kidney damage.

The test is available at DNA Labs UAE, a leading facility in genetic testing and diagnostics. The cost of the WDR19 gene nephronophthisis type 13 genetic test is 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in genetic analysis, ensuring accurate and reliable results. Patients seeking this test are usually referred by their healthcare provider, and it requires a sample of blood or saliva for analysis. The outcome of the test not only helps in the diagnosis but also aids in family planning and the assessment of risk for siblings and other family members.

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WDR19 Gene Nephronophthisis type 13 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 WDR19 Gene Nephronophthisis type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WDR19 Gene Nephronophthisis type 13 NGS Genetic DNA Test gene WDR19

Test Details

The WDR19 gene is associated with a rare genetic disorder called nephronophthisis type 13 (NPHP13). Nephronophthisis is a progressive kidney disease that typically starts in childhood and leads to end-stage renal disease (kidney failure) by early adulthood.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes. It is used to identify mutations or variations in genes that may be associated with certain genetic disorders, including NPHP13 caused by mutations in the WDR19 gene.

NGS genetic testing for the WDR19 gene in individuals suspected of having nephronophthisis type 13 can help confirm the diagnosis and provide important information for genetic counseling and family planning. It can also help with personalized treatment approaches and management of the disease.

It is important to note that genetic testing for NPHP13 and other genetic disorders should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Test Name WDR19 Gene Nephronophthisis type 13 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 WDR19 Gene Nephronophthisis type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WDR19 Gene Nephronophthisis type 13 NGS Genetic DNA Test gene WDR19
Test Details

The WDR19 gene is associated with a rare genetic disorder called nephronophthisis type 13 (NPHP13). Nephronophthisis is a progressive kidney disease that typically starts in childhood and leads to end-stage renal disease (kidney failure) by early adulthood.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes. It is used to identify mutations or variations in genes that may be associated with certain genetic disorders, including NPHP13 caused by mutations in the WDR19 gene.

NGS genetic testing for the WDR19 gene in individuals suspected of having nephronophthisis type 13 can help confirm the diagnosis and provide important information for genetic counseling and family planning. It can also help with personalized treatment approaches and management of the disease.

It is important to note that genetic testing for NPHP13 and other genetic disorders should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

SKU: TEST-3720 Category:

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