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CUBN Gene Megaloblastic Anemia Type 1 Finnish Type Genetic Test Cost

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

-21%

The “CUBN Gene Megaloblastic Anemia Type 1 Finnish Type Genetic Test” is a specialized diagnostic tool designed to identify mutations in the CUBN gene, which are responsible for a rare form of megaloblastic anemia, primarily observed in the Finnish population. This condition, known as Imerslund-Gräsbeck syndrome, leads to a deficiency in the absorption of vitamin B12, causing symptoms such as fatigue, weakness, and neurological issues due to ineffective red blood cell production.

The test involves analyzing the patient’s DNA to detect specific mutations in the CUBN gene that are indicative of this condition. It is a crucial step in diagnosing the disorder, allowing for appropriate management and treatment strategies to be implemented, which may include vitamin B12 supplementation.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the specialized nature of the analysis and the expertise required to interpret the results. This genetic test is particularly recommended for individuals of Finnish descent or those with a family history of megaloblastic anemia, as early detection can significantly improve the quality of life for affected individuals.

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CUBN Gene Megaloblastic Anemia Type 1 Finnish Type Genetic Test

Welcome to DNA Labs UAE’s blog on the CUBN Gene Megaloblastic Anemia Type 1 Finnish Type Genetic Test. In this blog, we will provide detailed information about the test, including its components, price, sample condition, report delivery time, method, test type, doctor, test department, pre-test information, and test details.

Test Name: CUBN Gene Megaloblastic Anemia Type 1 Finnish Type Genetic Test

Components: CUBN gene analysis

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

Prior to undergoing the CUBN Gene Megaloblastic Anemia Type 1 Finnish Type Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with the CUBN Gene Megaloblastic Anemia Type 1 Finnish Type NGS Genetic DNA Test gene CUBN.

Test Details

The CUBN gene is associated with megaloblastic anemia type 1, also known as the Finnish type. This condition is characterized by impaired absorption of vitamin B12 in the small intestine, leading to a deficiency of this essential nutrient.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, providing a comprehensive view of an individual’s genetic makeup. In the context of megaloblastic anemia type 1, NGS genetic testing can identify variations or mutations in the CUBN gene that may be responsible for the condition.

By analyzing the CUBN gene using NGS, healthcare professionals can determine if an individual carries any mutations that could lead to megaloblastic anemia type 1. This information can be useful for diagnosis, genetic counseling, and potentially guiding treatment decisions.

It’s important to note that genetic testing should be performed and interpreted by qualified healthcare professionals with expertise in genetics. They can provide appropriate guidance and support based on the results of the test.

Test Name CUBN Gene Megaloblastic anemia type 1 Finnish type 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 CUBN Gene Megaloblastic anemia type 1, Finnish type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CUBN Gene Megaloblastic anemia type 1, Finnish type NGS Genetic DNA Test gene CUBN
Test Details

The CUBN gene is associated with megaloblastic anemia type 1, also known as the Finnish type. This condition is characterized by impaired absorption of vitamin B12 in the small intestine, leading to a deficiency of this essential nutrient.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, providing a comprehensive view of an individual’s genetic makeup. In the context of megaloblastic anemia type 1, NGS genetic testing can identify variations or mutations in the CUBN gene that may be responsible for the condition.

By analyzing the CUBN gene using NGS, healthcare professionals can determine if an individual carries any mutations that could lead to megaloblastic anemia type 1. This information can be useful for diagnosis, genetic counseling, and potentially guiding treatment decisions.

It’s important to note that genetic testing should be performed and interpreted by qualified healthcare professionals with expertise in genetics. They can provide appropriate guidance and support based on the results of the test.

SKU: TEST-3925 Category:

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