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CPOX Gene Coproporphyria Genetic Test Cost

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

-21%

The CPOX Gene Coproporphyria Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the CPOX gene. These mutations are responsible for a condition known as Hereditary Coproporphyria (HCP), a rare type of porphyria that affects the body’s ability to produce heme, an essential component of hemoglobin. HCP is characterized by a range of symptoms including abdominal pain, neuropathy, and, in severe cases, neurological complications. The test, priced at 4400 AED, involves analyzing the patient’s DNA to detect specific genetic alterations in the CPOX gene, enabling precise diagnosis and facilitating appropriate management and treatment strategies for affected individuals. By identifying the genetic basis of the condition, this test plays a crucial role in the clinical approach to managing Hereditary Coproporphyria, offering hope for better outcomes through personalized medicine.

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CPOX Gene Coproporphyria Genetic Test

Welcome to DNA Labs UAE, where we offer the CPOX Gene Coproporphyria Genetic Test. This test is designed to analyze the CPOX gene for mutations associated with coproporphyria, a rare genetic disorder that affects the production of heme in the body.

Test Components and Price

The CPOX Gene Coproporphyria 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.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the analysis of multiple genes simultaneously.

Test Type and Department

The CPOX Gene Coproporphyria Genetic Test falls under the category of Metabolic Disorders. It is conducted in our Genetics department.

Referring Doctor and Pre-Test Information

A General Physician can refer patients for this test. Prior to the test, it is recommended 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 Coproporphyria.

Test Details

Coproporphyria is a rare genetic disorder that can lead to the accumulation of certain chemicals in the body. This can result in symptoms such as abdominal pain, neurological problems, and sensitivity to sunlight. The CPOX Gene Coproporphyria Genetic Test analyzes the CPOX gene for mutations associated with this disorder.

NGS (Next-Generation Sequencing) technology is used to sequence the CPOX gene and identify any mutations or variations. This test can help diagnose coproporphyria, identify individuals at risk, and determine carrier status in individuals with a family history of the disorder.

The results of the genetic test are crucial for healthcare providers to develop personalized treatment plans and provide genetic counseling to affected individuals and families.

For more information about the CPOX Gene Coproporphyria Genetic Test or to schedule an appointment, please contact DNA Labs UAE.

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

CPOX gene coproporphyria NGS genetic testing is a type of genetic test that analyzes the CPOX gene for mutations associated with coproporphyria. Coproporphyria is a rare genetic disorder that affects the production of heme, a component of hemoglobin. This disorder can lead to the buildup of certain chemicals in the body, causing symptoms such as abdominal pain, neurological problems, and sensitivity to sunlight.

NGS stands for next-generation sequencing, which is a high-throughput method used to analyze multiple genes simultaneously. In the case of CPOX gene coproporphyria NGS genetic testing, it involves sequencing the CPOX gene to identify any mutations or variations that may be present.

This type of genetic testing can help diagnose coproporphyria and identify individuals who may be at risk of developing the disorder. It can also be used to determine carrier status in individuals with a family history of coproporphyria.

The results of the genetic test can provide important information for healthcare providers to develop personalized treatment plans and provide genetic counseling to individuals and families affected by coproporphyria.