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HGD Gene Alkaptonuria Genetic Test Cost

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

-21%

The HGD Gene Alkaptonuria Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the HGD gene, which is responsible for alkaptonuria. Alkaptonuria is a rare inherited disorder that causes the body to be unable to properly break down certain amino acids, leading to a buildup of homogentisic acid in the body. This can result in darkening of the urine, arthritis, heart disease, and other complications.

The test is crucial for early detection and management of the condition, allowing for interventions that can significantly improve the quality of life for those affected. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the HGD gene that are known to cause alkaptonuria.

At DNA Labs UAE, the cost for the HGD Gene Alkaptonuria Genetic Test is set at 4400 AED. This price includes the full testing process, from sample collection to the comprehensive analysis and final report detailing the findings. It’s important for individuals with a family history of alkaptonuria or those experiencing symptoms to consider this test, as early detection is key to managing the disease effectively.

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HGD Gene Alkaptonuria Genetic Test

At DNA Labs UAE, we offer the HGD Gene Alkaptonuria Genetic Test for the diagnosis of alkaptonuria, a rare metabolic disorder caused by mutations in the HGD gene. This test can provide valuable information about an individual’s genetic makeup and help in the diagnosis and management of the condition.

Test Components and Price

The HGD Gene Alkaptonuria Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card for analysis.

Report Delivery

The test results are usually delivered within 3 to 4 weeks after the sample is received.

Test Method

The HGD Gene Alkaptonuria Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze the HGD gene for mutations associated with alkaptonuria. This advanced sequencing technique allows for the comprehensive assessment of an individual’s genetic makeup.

Test Type and Department

The HGD Gene Alkaptonuria Genetic Test falls under the category of Metabolic Disorders and is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is recommended to provide the clinical history of the patient who is undergoing the HGD Gene Alkaptonuria Genetic Test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by Alkaptonuria.

About Alkaptonuria

Alkaptonuria is an autosomal recessive disorder caused by mutations in the HGD gene. It is characterized by the accumulation of homogentisic acid (HGA) in the body, leading to various health problems. Symptoms of alkaptonuria include darkening of the urine, ochronosis (darkening of connective tissues such as cartilage and skin), arthritis, and kidney stones.

NGS Genetic Testing for Alkaptonuria

NGS genetic testing allows for the analysis of the entire HGD gene or specific regions of interest to identify any genetic variations or mutations associated with alkaptonuria. This type of testing provides a comprehensive assessment of an individual’s genetic makeup and can help in the diagnosis of the condition, confirmation of carrier status in family members, and genetic counseling.

Prenatal Testing

NGS genetic testing for alkaptonuria can also be used for prenatal testing to determine if a fetus is affected by the disorder. This information can help parents make informed decisions about their pregnancy and plan for appropriate medical care.

Importance of Qualified Healthcare Professionals

It is crucial to have the HGD Gene Alkaptonuria Genetic Test performed by a qualified healthcare professional or genetic counselor who can interpret the results accurately and provide appropriate guidance and support. They can help individuals and families understand the implications of the test results and assist in making informed decisions regarding their health and future.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule an appointment for the HGD Gene Alkaptonuria Genetic Test and take a step towards understanding your genetic makeup.

Test Name HGD Gene Alkaptonuria 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 HGD Gene Alkaptonuria NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Alkaptonuria
Test Details

The HGD gene is responsible for encoding an enzyme called homogentisate 1,2-dioxygenase. Mutations in this gene can lead to a rare metabolic disorder called alkaptonuria.

Alkaptonuria is an autosomal recessive disorder characterized by the accumulation of a substance called homogentisic acid (HGA) in the body. This acid can build up and cause a variety of health problems, including darkening of the urine, ochronosis (darkening of connective tissues such as cartilage and skin), arthritis, and kidney stones.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the HGD gene for mutations associated with alkaptonuria. This type of testing involves sequencing the entire gene or specific regions of interest to identify any genetic variations or mutations. NGS technology allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup.

Genetic testing for alkaptonuria can help diagnose individuals with the condition, confirm carrier status in family members, and provide information for genetic counseling. It can also be used for prenatal testing to determine if a fetus is affected by the disorder.

It’s important to note that genetic testing for alkaptonuria should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.