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. |