HPD Gene Tyrosinemia type 3 Genetic Test sale cost 4400 AED
TPI1 Gene Triosephosphate isomerase deficiency Genetic Test sale cost 4400 AED TPI1 Gene Triosephosphate isomerase deficiency Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
GI Gastrointestinal Panel Stool Test sale cost 4680 AED GI Gastrointestinal Panel Stool Test Cost 5,200 د.إ Original price was: 5,200 د.إ.4,680 د.إCurrent price is: 4,680 د.إ.
Sale!

HPD Gene Tyrosinemia type 3 Genetic Test Cost

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

-21%

The HPD Gene Tyrosinemia Type 3 Genetic Test is a specialized diagnostic procedure designed to detect mutations in the HPD gene, which are associated with Tyrosinemia type 3, a rare metabolic disorder. This condition results from the body’s inability to effectively break down the amino acid tyrosine, leading to various health issues, including intellectual disabilities, seizures, and liver problems. Early detection through this genetic test can enable timely intervention and management of the condition, potentially mitigating severe outcomes. The test is available at DNA Labs UAE, a leading facility in genetic diagnostics, offering the test at a cost of 4400 AED. This test is crucial for individuals with a family history of Tyrosinemia or those showing symptoms related to the disorder, providing them with essential insights into their genetic health.

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

HPD Gene Tyrosinemia type 3 Genetic Test

At DNA Labs UAE, we offer the HPD Gene Tyrosinemia type 3 Genetic Test for individuals who suspect they may have this rare genetic disorder. This test can help diagnose Tyrosinemia type 3 and provide important information for genetic counseling and family planning.

Test Details

The HPD gene is responsible for producing an enzyme called 4-hydroxyphenylpyruvate dioxygenase (HPD), which is crucial for the breakdown of the amino acid tyrosine. Tyrosinemia type 3 is characterized by a deficiency in the HPD enzyme.

Our NGS (Next-Generation Sequencing) Genetic Test allows for the rapid and comprehensive analysis of multiple genes simultaneously. In the case of Tyrosinemia type 3, this test can identify mutations or variations in the HPD gene that may be responsible for the disorder.

Test Components and Price

Test Name: HPD Gene Tyrosinemia type 3 Genetic Test

  • Components: NGS Technology
  • Price: 4400.0 AED

Sample Condition

We accept the following sample conditions for this test:

  • Blood
  • Extracted DNA
  • One drop of blood on FTA Card

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Doctor and Test Department

This test can be ordered by a General Physician and is conducted in our Genetics department.

Pre Test Information

Before undergoing the HPD Gene Tyrosinemia type 3 Genetic Test, it is recommended to provide the following:

  • Clinical history of the patient
  • Genetic counseling session to draw a pedigree chart of family members affected with Tyrosinemia type 3

Benefits of NGS Genetic Testing

NGS Genetic Testing for Tyrosinemia type 3 offers several benefits:

  • Identifying individuals at risk for the condition
  • Allowing for early detection and intervention
  • Providing information for genetic counseling and family planning

Don’t wait, get tested today at DNA Labs UAE!

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

The HPD gene is responsible for producing an enzyme called 4-hydroxyphenylpyruvate dioxygenase (HPD), which plays a crucial role in the breakdown of an amino acid called tyrosine. Tyrosinemia type 3 is a rare genetic disorder characterized by a deficiency in the HPD enzyme.

NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing technique that allows for the rapid and comprehensive analysis of multiple genes simultaneously. In the context of Tyrosinemia type 3, an NGS Genetic Test can be used to identify mutations or variations in the HPD gene that may be responsible for the disorder.

This genetic test involves obtaining a DNA sample, typically through a blood sample, from the individual being tested. The DNA is then sequenced using NGS technology, which can detect variations in the HPD gene. The results of the test can help confirm a diagnosis of Tyrosinemia type 3 and provide information about the specific genetic mutation causing the disorder.

NGS Genetic Testing for Tyrosinemia type 3 can be helpful in identifying individuals at risk for the condition, allowing for early detection and intervention. It can also provide important information for genetic counseling and family planning.

SKU: TEST-2652 Category:

Related products