GRHPR Gene Hyperoxaluria Type 2 Genetic Test sale cost 4400 AED
APOB Gene Hypercholesterolemia Type B Autosomal Dominant Genetic Test sale cost 4400 AED APOB Gene Hypercholesterolemia Type B Autosomal Dominant Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
GALC Gene Krabbe Disease Genetic Test sale cost 4400 AED GALC Gene Krabbe Disease Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

GRHPR Gene Hyperoxaluria Type 2 Genetic Test Cost

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

-21%

The GRHPR Gene Hyperoxaluria Type 2 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the GRHPR gene, which are associated with Primary Hyperoxaluria Type 2 (PH2). PH2 is a rare genetic disorder characterized by the excessive production of oxalate, leading to kidney stones, nephrocalcinosis, and potentially kidney failure. This condition is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

DNA Labs UAE offers this crucial genetic test, which is conducted through a blood sample or a cheek swab to extract DNA for analysis. The test specifically looks for mutations in the GRHPR gene that are known to cause PH2, providing valuable information for diagnosis, treatment planning, and genetic counseling. It is particularly important for individuals with a family history of Primary Hyperoxaluria or related symptoms, and for couples considering having children who may want to know their carrier status.

The cost of the GRHPR Gene Hyperoxaluria Type 2 Genetic Test at DNA Labs UAE is 4400 AED. This investment can provide critical insights for affected individuals and their families, enabling early and effective management of the condition. Early diagnosis through genetic testing can significantly impact the quality of life and health outcomes for those with PH2 by allowing for tailored treatments that can reduce the production of oxalate and mitigate the risk of kidney damage.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

GRHPR Gene Hyperoxaluria type 2 Genetic Test

Test Name: GRHPR Gene Hyperoxaluria type 2 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 GRHPR Gene Hyperoxaluria type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperoxaluria type 2.

Test Details

The GRHPR gene is responsible for producing an enzyme called glyoxylate reductase/hydroxypyruvate reductase (GRHPR), which plays a crucial role in the metabolism of glyoxylate, a substance produced during the breakdown of certain amino acids. Mutations in the GRHPR gene can lead to a condition called hyperoxaluria type 2.

Hyperoxaluria type 2 is a rare genetic disorder characterized by the accumulation of oxalate, a byproduct of glyoxylate metabolism, in the body. This excess oxalate can form crystals and stones in the kidneys and other organs, leading to kidney damage and other complications.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify mutations or variants that may be associated with a particular condition. In the case of GRHPR gene hyperoxaluria type 2, NGS genetic testing can be used to identify mutations or variants in the GRHPR gene that may be responsible for the condition.

NGS genetic testing involves sequencing the DNA of an individual, usually obtained through a blood or saliva sample. The DNA sequence is then compared to a reference sequence to identify any differences or mutations in the GRHPR gene. This information can help in confirming a diagnosis of hyperoxaluria type 2 and may also be useful in genetic counseling and family planning.

It is important to note that NGS genetic testing may not be available at all healthcare facilities and may require a referral to a specialized genetic testing laboratory. Additionally, the interpretation of the test results should be done by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support.

Test Name GRHPR Gene Hyperoxaluria type 2 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 GRHPR Gene Hyperoxaluria type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperoxaluria type 2
Test Details

The GRHPR gene is responsible for producing an enzyme called glyoxylate reductase/hydroxypyruvate reductase (GRHPR), which plays a crucial role in the metabolism of glyoxylate, a substance produced during the breakdown of certain amino acids. Mutations in the GRHPR gene can lead to a condition called hyperoxaluria type 2.

Hyperoxaluria type 2 is a rare genetic disorder characterized by the accumulation of oxalate, a byproduct of glyoxylate metabolism, in the body. This excess oxalate can form crystals and stones in the kidneys and other organs, leading to kidney damage and other complications.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify mutations or variants that may be associated with a particular condition. In the case of GRHPR gene hyperoxaluria type 2, NGS genetic testing can be used to identify mutations or variants in the GRHPR gene that may be responsible for the condition.

NGS genetic testing involves sequencing the DNA of an individual, usually obtained through a blood or saliva sample. The DNA sequence is then compared to a reference sequence to identify any differences or mutations in the GRHPR gene. This information can help in confirming a diagnosis of hyperoxaluria type 2 and may also be useful in genetic counseling and family planning.

It is important to note that NGS genetic testing may not be available at all healthcare facilities and may require a referral to a specialized genetic testing laboratory. Additionally, the interpretation of the test results should be done by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support.

SKU: TEST-2452 Category:

Related products