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XDH Gene Xanthinuria type 1 Genetic Test Cost

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

-21%

The XDH Gene Xanthinuria Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the XDH gene that are associated with Xanthinuria Type 1. This rare genetic disorder impacts the body’s ability to metabolize purines, leading to an accumulation of xanthine, which can result in kidney stones, kidney failure, and occasionally muscle disease. The test involves analyzing the patient’s DNA to identify any genetic alterations in the XDH gene that might lead to the condition. With a cost of 4400 AED, the test provides crucial information for the accurate diagnosis and management of Xanthinuria Type 1, enabling targeted treatment plans and lifestyle adjustments to mitigate the risk of complications associated with this disorder. DNA Labs UAE, known for its advanced genetic testing services, offers this test as part of its commitment to providing comprehensive diagnostic solutions for rare genetic conditions.

Description

XDH Gene Xanthinuria type 1 Genetic Test

Test Name: XDH Gene Xanthinuria type 1 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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for XDH Gene Xanthinuria type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Xanthinuria type 1.

Test Details:

The XDH gene is associated with Xanthinuria type 1, which is a rare genetic disorder characterized by the inability to break down xanthine, a waste product of purine metabolism. This results in the accumulation of xanthine in the urine and can lead to kidney stones and other urinary tract problems.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes. In the case of Xanthinuria type 1, NGS genetic testing can be used to identify mutations or variations in the XDH gene that are associated with the condition. By analyzing the DNA sequence of the XDH gene, NGS genetic testing can help diagnose Xanthinuria type 1 in individuals with symptoms or a family history of the disorder. It can also be used for carrier testing in individuals who have a family history of the condition but do not show any symptoms themselves.

NGS genetic testing for Xanthinuria type 1 typically involves obtaining a DNA sample, usually through a blood or saliva sample, and then sequencing the XDH gene to identify any mutations or variations. The results of the test can help guide treatment and management options for individuals with Xanthinuria type 1.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate counseling and support.

Test Name	XDH Gene Xanthinuria type 1 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	Metabolic Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for XDH Gene Xanthinuria type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Xanthinuria type 1
Test Details	The XDH gene is associated with Xanthinuria type 1, which is a rare genetic disorder characterized by the inability to break down xanthine, a waste product of purine metabolism. This results in the accumulation of xanthine in the urine and can lead to kidney stones and other urinary tract problems. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes. In the case of Xanthinuria type 1, NGS genetic testing can be used to identify mutations or variations in the XDH gene that are associated with the condition. By analyzing the DNA sequence of the XDH gene, NGS genetic testing can help diagnose Xanthinuria type 1 in individuals with symptoms or a family history of the disorder. It can also be used for carrier testing in individuals who have a family history of the condition but do not show any symptoms themselves. NGS genetic testing for Xanthinuria type 1 typically involves obtaining a DNA sample, usually through a blood or saliva sample, and then sequencing the XDH gene to identify any mutations or variations. The results of the test can help guide treatment and management options for individuals with Xanthinuria type 1. It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate counseling and support.