The HLA B51 test is a genetic analysis designed to detect the presence of the HLA B51 allele, a marker linked to autoimmune conditions, particularly Behçet's disease. This chronic disorder is characterized by recurrent ulcers, skin lesions, and eye inflammation. The test is instrumental in diagnosing Behçet's disease, offering genetic insights that aid in disease management and treatment planning. Additionally, it plays a crucial role in organ and tissue transplantation by assessing donor-recipient compatibility, thereby reducing the risk of rejection. The test also evaluates the risk of other autoimmune diseases associated with the HLA B51 allele. It requires blood or buccal swab samples and employs methodologies like PCR and massively parallel sequencing. With a turnaround time of 5 to 7 business days, the test boasts high specificity but should be used alongside other diagnostic tools due to its limitations. A positive result indicates an increased risk for Behçet's disease, guiding clinicians in patient management.
The HLA B51 test is a genetic analysis designed to detect the presence of the HLA B51 allele, a marker linked to autoimmune conditions, particularly Behçet's disease. This chronic disorder is characterized by recurrent ulcers, skin lesions, and eye inflammation. The test is instrumental in diagnosing Behçet's disease, offering genetic insights that aid in disease management and treatment planning. Additionally, it plays a crucial role in organ and tissue transplantation by assessing donor-recipient compatibility, thereby reducing the risk of rejection. The test also evaluates the risk of other autoimmune diseases associated with the HLA B51 allele. It requires blood or buccal swab samples and employs methodologies like PCR and massively parallel sequencing. With a turnaround time of 5 to 7 business days, the test boasts high specificity but should be used alongside other diagnostic tools due to its limitations. A positive result indicates an increased risk for Behçet's disease, guiding clinicians in patient management.
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The HLA B51 test is a genetic analysis used to identify the presence of the HLA B51 allele, linked to autoimmune conditions like Behçet's disease. This test is essential for:
- Diagnosing Behçet's disease by identifying genetic predisposition.
- Assessing organ and tissue transplant compatibility to reduce rejection risk.
- Evaluating autoimmune disease risk associated with the HLA B51 allele.
Sample requirements include blood or buccal swabs. Methods like PCR and SSOP are used, with results in 5-7 days. Despite its utility, the test isn't solely diagnostic and should be used alongside other evaluations.
The HLA B51 test is essential for identifying individuals at risk for autoimmune diseases, particularly Behçet's disease. It aids in diagnosis and treatment planning by detecting the HLA B51 allele. Key indications include:
- Behçet's Disease Diagnosis: Recommended for suspected cases, as it indicates increased predisposition.
- Organ and Tissue Transplantation: Ensures compatibility, reducing rejection risk.
- Autoimmune Disease Risk Assessment: Evaluates risk for other conditions linked to HLA B51.
The test uses blood or buccal swabs, with results in 5-7 days, offering high specificity and sensitivity.
Understanding test results is crucial for informed decision-making. Here's a concise guide:
- Positive Result: Indicates the presence of the HLA B51 allele, suggesting an increased risk for Behçet's disease and potential autoimmune conditions. It aids in early diagnosis and treatment planning.
- Negative Result: Suggests a lower likelihood of Behçet's disease but doesn't rule out other autoimmune disorders.
- Transplant Compatibility: A matching HLA B51 status between donor and recipient reduces rejection risk.
- Consultation: Always discuss results with a healthcare provider for comprehensive interpretation and next steps.
The lowest price from the last 30 days: £282
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