Sale!

FAN1 Gene Interstitial Nephritis Karyomegalic Genetic Test Cost

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

-21%

The FAN1 Gene Interstitial Nephritis Karyomegalic Genetic Test is a specialized diagnostic tool designed to identify mutations in the FAN1 gene, which are linked to Karyomegalic Interstitial Nephritis (KIN), a rare genetic disorder. This condition is characterized by chronic kidney disease, where the kidneys show abnormal enlargement of the nuclei in the renal tubular cells, leading to progressive renal failure. Early diagnosis through genetic testing is crucial for managing the disease’s progression and exploring potential treatment options.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the patient’s DNA to detect any genetic abnormalities associated with KIN. Given the complexity and the specialized nature of this test, it is priced at 4400 AED. This test is vital for individuals with a family history of KIN or those showing symptoms related to kidney dysfunction, as it provides a definitive diagnosis, enabling healthcare providers to tailor a management plan that could include monitoring kidney function, managing symptoms, and possibly considering genetic counseling for affected families.

Description

FAN1 Gene Interstitial Nephritis Karyomegalic Genetic Test

Test Name: FAN1 Gene Interstitial Nephritis Karyomegalic 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 FAN1 Gene Interstitial Nephritis Karyomegalic NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FAN1 Gene Interstitial Nephritis Karyomegalic NGS Genetic DNA Test gene FAN1

Test Details: The FAN1 gene is associated with a condition called karyomegalic interstitial nephritis (KIN). KIN is a rare genetic disorder characterized by inflammation and enlargement of the kidneys’ interstitial tissue. It can lead to kidney dysfunction and eventually kidney failure. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that analyzes multiple genes simultaneously. It can identify mutations or variations in the FAN1 gene that may be responsible for causing KIN. Genetic testing for KIN can help confirm a diagnosis, determine the specific genetic mutation causing the condition, and provide information for genetic counseling and family planning. It can also be used to identify family members who may be at risk of developing KIN. It is important to consult with a healthcare professional or a genetic counselor to discuss the specific details and implications of undergoing a genetic test for the FAN1 gene and KIN. They can provide more personalized information and guidance based on your individual situation.

Test Name	FAN1 Gene Interstitial nephritis karyomegalic 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 FAN1 Gene Interstitial nephritis karyomegalic NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FAN1 Gene Interstitial nephritis karyomegalic NGS Genetic DNA Test gene FAN1
Test Details	The FAN1 gene is associated with a condition called karyomegalic interstitial nephritis (KIN). KIN is a rare genetic disorder characterized by inflammation and enlargement of the kidneys’ interstitial tissue. It can lead to kidney dysfunction and eventually kidney failure. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that analyzes multiple genes simultaneously. It can identify mutations or variations in the FAN1 gene that may be responsible for causing KIN. Genetic testing for KIN can help confirm a diagnosis, determine the specific genetic mutation causing the condition, and provide information for genetic counseling and family planning. It can also be used to identify family members who may be at risk of developing KIN. It is important to consult with a healthcare professional or a genetic counselor to discuss the specific details and implications of undergoing a genetic test for the FAN1 gene and KIN. They can provide more personalized information and guidance based on your individual situation.