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C15orf41 Gene Dyserythropoietic Anemia Congenital Type 1B Genetic Test

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

-21%

The C15orf41 gene plays a crucial role in human genetics, particularly in the context of dyserythropoietic anemia congenital type 1B, a rare blood disorder characterized by ineffective erythropoiesis leading to anemia. The condition is genetically inherited and involves abnormalities in red blood cell formation, causing various symptoms such as fatigue, pallor, and in severe cases, skeletal deformations and growth retardation.

A genetic test for this condition focuses on identifying mutations in the C15orf41 gene, which can confirm a diagnosis of dyserythropoietic anemia congenital type 1B. This is crucial for the management and treatment of the condition, as well as for genetic counseling of affected families.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately detect and interpret mutations in the C15orf41 gene. This test is essential for individuals showing symptoms of the condition or those with a family history, providing them with critical information for managing their health.

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C15orf41 Gene Dyserythropoietic Anemia Congenital Type 1B Genetic Test

At DNA Labs UAE, we offer the C15orf41 Gene Dyserythropoietic Anemia Congenital Type 1B Genetic Test. This test is designed to diagnose and identify mutations or variations in the C15orf41 gene that may be causing dyserythropoietic anemia, congenital, type 1B.

Test Details

The C15orf41 gene is associated with dyserythropoietic anemia, congenital, type 1B. This rare genetic disorder is characterized by abnormal development of red blood cells, leading to anemia. By analyzing the C15orf41 gene using NGS (Next-Generation Sequencing) technology, our healthcare professionals can determine if an individual has any disease-causing mutations in this gene.

Components

  • Test Name: C15orf41 Gene Dyserythropoietic Anemia Congenital Type 1B 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

Prior to the C15orf41 Gene Dyserythropoietic Anemia Congenital Type 1B 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 dyserythropoietic anemia, congenital, type 1B.

Benefits of NGS Genetic Testing

NGS genetic testing allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of dyserythropoietic anemia, congenital, type 1B, NGS genetic testing can help identify mutations or variations in the C15orf41 gene that may be causing the condition. This information is valuable for the diagnosis, management, and genetic counseling of individuals and families affected by dyserythropoietic anemia, congenital, type 1B.

At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. Our team of experts, including hematologists and geneticists, are dedicated to helping individuals and families understand their genetic makeup and make informed decisions regarding their health.

For more information or to schedule a C15orf41 Gene Dyserythropoietic Anemia Congenital Type 1B Genetic Test, please contact our genetics department.

Test Name C15orf41 Gene Dyserythropoietic anemia congenital type 1B 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 C15orf41 Gene Dyserythropoietic anemia, congenital, type 1B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with C15orf41 Gene Dyserythropoietic anemia, congenital, type 1B NGS Genetic DNA Test gene C15orf41
Test Details

The C15orf41 gene is associated with a condition called dyserythropoietic anemia, congenital, type 1B. This is a rare genetic disorder characterized by abnormal development of red blood cells, leading to anemia.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of dyserythropoietic anemia, congenital, type 1B, NGS genetic testing can be used to identify mutations or variations in the C15orf41 gene that may be causing the condition.

By analyzing the C15orf41 gene using NGS, healthcare professionals can determine if an individual has any disease-causing mutations in this gene. This information can help with the diagnosis, management, and genetic counseling of individuals and families affected by dyserythropoietic anemia, congenital, type 1B.

SKU: TEST-3894 Category:

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