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HOGA1 Gene Hyperoxaluria Type 3 Genetic Test Cost

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

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The HOGA1 Gene Hyperoxaluria Type 3 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the HOGA1 gene, which are responsible for Type 3 Primary Hyperoxaluria (PH3). This rare genetic disorder affects the body’s ability to properly metabolize glyoxylate, leading to the excessive production and accumulation of oxalate. The excessive oxalate can then combine with calcium to form calcium oxalate crystals, which can deposit in the kidneys and other organs, potentially leading to kidney stones, nephrocalcinosis, and even chronic kidney disease.

The test is particularly vital for individuals showing symptoms of kidney stones, recurrent urinary tract infections, or those with a family history of Primary Hyperoxaluria, as early detection can significantly influence the management and treatment of the condition. Conducted through a blood sample or cheek swab, the genetic test seeks to identify specific mutations in the HOGA1 gene that are indicative of Type 3 Primary Hyperoxaluria.

At DNA Labs UAE, the cost for the HOGA1 Gene Hyperoxaluria Type 3 Genetic Test is set at 4400 AED. The test is performed under stringent laboratory conditions by experienced geneticists and medical professionals, ensuring accurate and reliable results. By opting for this test, patients and healthcare providers can make informed decisions regarding the management of the condition, potentially mitigating severe complications associated with the disorder.

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HOGA1 Gene Hyperoxaluria type 3 Genetic Test

Test Name: HOGA1 Gene Hyperoxaluria type 3 Genetic Test

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

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 HOGA1 Gene Hyperoxaluria type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperoxaluria type 3.

Test Details

The HOGA1 gene is associated with a condition called Hyperoxaluria type 3. Hyperoxaluria is a genetic disorder characterized by the excessive production and accumulation of a substance called oxalate in the body. This can lead to the formation of kidney stones and other complications.

NGS (Next-Generation Sequencing) Genetic Testing is a method used to analyze multiple genes simultaneously to identify any variations or mutations that may be present. In the case of Hyperoxaluria type 3, NGS testing can be used to analyze the HOGA1 gene to identify any genetic variations or mutations that may be causing the condition.

By identifying the specific genetic mutation causing Hyperoxaluria type 3, NGS testing can help in the diagnosis of the condition, provide information on the severity of the disease, and guide treatment options. It can also be useful for genetic counseling and family planning purposes.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on the individual’s specific situation.

Test Name HOGA1 Gene Hyperoxaluria type 3 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 HOGA1 Gene Hyperoxaluria type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperoxaluria type 3
Test Details

The HOGA1 gene is associated with a condition called Hyperoxaluria type 3. Hyperoxaluria is a genetic disorder characterized by the excessive production and accumulation of a substance called oxalate in the body. This can lead to the formation of kidney stones and other complications.

NGS (Next-Generation Sequencing) Genetic Testing is a method used to analyze multiple genes simultaneously to identify any variations or mutations that may be present. In the case of Hyperoxaluria type 3, NGS testing can be used to analyze the HOGA1 gene to identify any genetic variations or mutations that may be causing the condition.

By identifying the specific genetic mutation causing Hyperoxaluria type 3, NGS testing can help in the diagnosis of the condition, provide information on the severity of the disease, and guide treatment options. It can also be useful for genetic counseling and family planning purposes.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on the individual’s specific situation.

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