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EPOR Gene Erythrocytosis Familial Type 1 Genetic Test

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

-21%

The EPOR Gene Erythrocytosis Familial Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the EPOR gene. These mutations are associated with Familial Erythrocytosis Type 1, a rare condition characterized by an increased number of red blood cells due to overproduction. This genetic anomaly leads to a high hemoglobin concentration, which can cause a range of symptoms from mild to severe, including headaches, dizziness, and an increased risk of thrombosis.

This test is crucial for individuals with a family history of the condition or those exhibiting symptoms, as early detection can lead to better management of the condition. Conducted at DNA Labs UAE, a facility known for its state-of-the-art technology and expertise in genetic diagnostics, the test ensures accuracy and reliability.

The cost of the EPOR Gene Erythrocytosis Familial Type 1 Genetic Test is set at 4400 AED. This investment covers the comprehensive analysis required to detect any mutations in the EPOR gene, providing essential information for the proper management and treatment of the condition.

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EPOR Gene Erythrocytosis familial type 1 Genetic Test

Components

  • Test Name: EPOR Gene Erythrocytosis familial type 1 Genetic Test
  • 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: Hematology
  • Doctor: Hematologist
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for EPOR Gene Erythrocytosis, familial type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EPOR Gene Erythrocytosis, familial type 1 NGS Genetic DNA Test gene EPOR.

Test Details

The EPOR gene erythrocytosis, familial type 1 NGS genetic test is a genetic test that is used to identify mutations in the EPOR gene that are associated with familial erythrocytosis type 1. Erythrocytosis is a condition characterized by an excessive production of red blood cells in the body. It can lead to an increase in blood viscosity, which can cause symptoms such as headache, dizziness, and fatigue. Familial erythrocytosis type 1 is a rare form of erythrocytosis that is inherited in an autosomal dominant manner, meaning that a person only needs to inherit one copy of the mutated EPOR gene from either parent to develop the condition. The EPOR gene provides instructions for making a protein called erythropoietin receptor, which is involved in the regulation of red blood cell production. Mutations in the EPOR gene can lead to a malfunctioning erythropoietin receptor, causing the body to produce too many red blood cells. The NGS (Next-Generation Sequencing) genetic test involves analyzing the DNA sequence of the EPOR gene to identify any mutations or variations that may be present. This test can help confirm a diagnosis of familial erythrocytosis type 1 and can also be used for genetic counseling and family planning purposes. Overall, the EPOR gene erythrocytosis, familial type 1 NGS genetic test is a valuable tool in the diagnosis and management of familial erythrocytosis type 1, allowing for early detection, accurate diagnosis, and appropriate treatment of affected individuals.

Test Name EPOR Gene Erythrocytosis familial type 1 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 Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for EPOR Gene Erythrocytosis, familial type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EPOR Gene Erythrocytosis, familial type 1 NGS Genetic DNA Test gene EPOR
Test Details

EPOR gene erythrocytosis, familial type 1 NGS genetic test is a genetic test that is used to identify mutations in the EPOR gene that are associated with familial erythrocytosis type 1.

Erythrocytosis is a condition characterized by an excessive production of red blood cells in the body. It can lead to an increase in blood viscosity, which can cause symptoms such as headache, dizziness, and fatigue. Familial erythrocytosis type 1 is a rare form of erythrocytosis that is inherited in an autosomal dominant manner, meaning that a person only needs to inherit one copy of the mutated EPOR gene from either parent to develop the condition.

The EPOR gene provides instructions for making a protein called erythropoietin receptor, which is involved in the regulation of red blood cell production. Mutations in the EPOR gene can lead to a malfunctioning erythropoietin receptor, causing the body to produce too many red blood cells.

The NGS (Next-Generation Sequencing) genetic test involves analyzing the DNA sequence of the EPOR gene to identify any mutations or variations that may be present. This test can help confirm a diagnosis of familial erythrocytosis type 1 and can also be used for genetic counseling and family planning purposes.

Overall, the EPOR gene erythrocytosis, familial type 1 NGS genetic test is a valuable tool in the diagnosis and management of familial erythrocytosis type 1, allowing for early detection, accurate diagnosis, and appropriate treatment of affected individuals.

SKU: TEST-3898 Category:

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