Sale!

PHEX Gene Hypophosphatemic rickets X-linked Genetic Test Cost

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

-21%

The PHEX Gene Hypophosphatemic Rickets X-Linked Genetic Test is a specialized diagnostic procedure designed to identify mutations in the PHEX gene, which are known to cause X-linked hypophosphatemic rickets (XLH). XLH is a genetic disorder characterized by low levels of phosphate in the blood, leading to weak and soft bones, potentially resulting in bone deformities and other related health issues. This condition is inherited in an X-linked dominant pattern, meaning it can affect both males and females, but males often experience more severe symptoms.

The test is performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities. By analyzing a patient’s DNA, the test can confirm the presence of mutations in the PHEX gene, providing crucial information for the diagnosis and management of XLH. Early detection through genetic testing can enable targeted treatment strategies, including phosphate supplements and vitamin D therapy, to manage symptoms and improve quality of life.

The cost of the PHEX Gene Hypophosphatemic Rickets X-Linked Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of obtaining a precise diagnosis to guide effective treatment and management of this condition cannot be understated. For families and individuals at risk of XLH, this test represents a critical step towards understanding and addressing this genetic disorder.

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

PHEX Gene Hypophosphatemic Rickets X-linked Genetic Test

At DNA Labs UAE, we offer the PHEX Gene Hypophosphatemic Rickets X-linked Genetic Test to help diagnose and manage this genetic disorder. This test is specifically designed to analyze the PHEX gene, which is associated with hypophosphatemic rickets.

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: Osteology Dermatology Immunology Disorders

Doctor and Test Department

This test is conducted by our experienced Dermatologist and is performed in our Genetics department.

Pre Test Information

Before undergoing the PHEX Gene Hypophosphatemic Rickets X-linked Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by this genetic disorder.

Test Details

Hypophosphatemic rickets is a condition characterized by low levels of phosphate in the blood, resulting in impaired bone mineralization and skeletal abnormalities. The PHEX gene is associated with this X-linked genetic disorder.

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously. In the case of hypophosphatemic rickets, NGS genetic testing helps identify mutations or variations in the PHEX gene that may be responsible for the condition.

During the test, a blood or saliva sample is obtained from the individual being tested. The DNA is then extracted and sequenced using NGS technology in our laboratory. The resulting data is analyzed to identify any mutations or variations in the PHEX gene associated with hypophosphatemic rickets.

NGS genetic testing has revolutionized the field of genetics by allowing for the simultaneous analysis of multiple genes at a faster and more cost-effective rate compared to traditional sequencing methods. This has greatly improved the diagnosis and understanding of genetic disorders, including hypophosphatemic rickets.

If you suspect that you or a family member may have hypophosphatemic rickets, our PHEX Gene Hypophosphatemic Rickets X-linked Genetic Test can provide valuable insights for diagnosis, genetic counseling, and management of the disorder.

Test Name PHEX Gene Hypophosphatemic rickets X-linked 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PHEX Gene Hypophosphatemic rickets, X-linked NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PHEX Gene Hypophosphatemic rickets, X-linked NGS Genetic DNA Test gene PHEX
Test Details

The PHEX gene is associated with a condition called hypophosphatemic rickets, which is an X-linked genetic disorder. Hypophosphatemic rickets is characterized by low levels of phosphate in the blood, leading to impaired bone mineralization and skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of hypophosphatemic rickets, NGS genetic testing can be used to identify mutations or variations in the PHEX gene that may be responsible for the condition.

NGS genetic testing involves sequencing the DNA of an individual to identify specific variations or mutations in genes associated with a particular disorder. In the case of hypophosphatemic rickets, NGS testing can help in diagnosing the condition, determining the specific genetic mutation responsible, and providing information for genetic counseling and management of the disorder.

The NGS genetic test for PHEX gene mutations may involve obtaining a blood or saliva sample from the individual being tested. The sample is then sent to a laboratory where the DNA is extracted and sequenced using NGS technology. The resulting data is analyzed to identify any mutations or variations in the PHEX gene that may be associated with hypophosphatemic rickets.

NGS genetic testing has revolutionized the field of genetics by allowing for the simultaneous analysis of multiple genes at a much faster and more cost-effective rate compared to traditional sequencing methods. This has significantly improved the diagnosis and understanding of genetic disorders, including hypophosphatemic rickets.