C3 Gene C3 deficiency Genetic Test
Welcome to DNA Labs UAE’s blog on C3 Gene C3 deficiency Genetic Test. In this blog, we will discuss the cost, symptoms, diagnosis, and other important details about this test.
Test Details
The C3 gene is responsible for producing the C3 protein, which plays a crucial role in the immune system’s complement pathway. Deficiency in the C3 gene can lead to a condition called C3 deficiency, where the body is unable to effectively combat infections.
The C3 deficiency Genetic Test is performed using NGS (Next-Generation Sequencing) technology. This high-throughput method allows for the sequencing of multiple genes simultaneously, providing a comprehensive view of the genetic makeup.
The test specifically focuses on sequencing the C3 gene to identify any variations or mutations that may be causing the deficiency. This information can help in diagnosing C3 deficiency and determining the appropriate treatment plan.
Test Components and Price
The cost of the C3 Gene C3 deficiency Genetic Test is AED 4400.0. The test can be performed using a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
The report for the C3 Gene C3 deficiency Genetic Test is typically delivered within 3 to 4 weeks. The test is conducted using NGS technology, which allows for efficient and accurate analysis of the genetic material.
Test Type and Doctor
The C3 Gene C3 deficiency Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. It is typically recommended to be performed by a dermatologist, as they specialize in disorders related to the skin and immune system.
Test Department
The C3 Gene C3 deficiency Genetic Test is conducted in the Genetics department of our lab. Our team of experts in genetics ensures accurate and reliable results.
Pre Test Information
Prior to undergoing the C3 Gene C3 deficiency 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 by C3 Gene C3 deficiency. This information helps in understanding the inheritance pattern and identifying potential carriers of the gene.
Conclusion
The C3 Gene C3 deficiency Genetic Test is a specialized test that analyzes the C3 gene to identify any variations or mutations causing the deficiency. It is recommended for individuals with suspected C3 deficiency or a family history of the condition. Consulting with a healthcare professional or genetic counselor is important to understand the implications of the test results and determine the most appropriate course of action.
| Test Name | C3 Gene C3 deficiency 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 C3 Gene C3 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with C3 Gene C3 deficiency NGS Genetic DNA Test gene C3 |
| Test Details |
C3 gene is responsible for producing the C3 protein, which plays a crucial role in the immune system’s complement pathway. Deficiency in the C3 gene can lead to a condition called C3 deficiency, where the body is unable to effectively combat infections. NGS (Next-Generation Sequencing) Genetic Test is a high-throughput method used to analyze the genetic material of an individual. It allows for the sequencing of multiple genes simultaneously, providing a comprehensive view of the genetic makeup. C3 deficiency NGS Genetic Test specifically focuses on sequencing the C3 gene to identify any variations or mutations that may be causing the deficiency. This test can help in diagnosing C3 deficiency and determining the appropriate treatment plan. The NGS Genetic Test involves collecting a sample, usually through a blood or saliva sample, from the individual. The DNA from the sample is then isolated and prepared for sequencing. Next-generation sequencing technology is used to analyze the DNA and identify any variations in the C3 gene. The results of the C3 deficiency NGS Genetic Test can provide valuable information about the specific genetic variations causing the deficiency. This information can help in understanding the underlying cause of the condition and guide treatment decisions. It is important to note that the C3 deficiency NGS Genetic Test is a specialized test and may not be routinely offered by all genetic testing laboratories. It is typically recommended for individuals with suspected C3 deficiency or a family history of the condition. It is always recommended to consult with a healthcare professional or a genetic counselor to understand the implications of the test results and to determine the most appropriate course of action. |
