Immunology Genetic Testing

Immunology genetic testing is a diagnostic tool that analyzes a person’s DNA to identify genetic variants affecting the immune system. It helps detect inherited immune disorders, autoimmune diseases, and conditions that compromise immune function. By examining specific genes related to immune regulation, the test can reveal abnormalities that impact how the body defends against infections or mistakenly attacks its own tissues. This testing is especially valuable in diagnosing rare primary immunodeficiencies and predicting disease risks. It also supports personalized treatment planning and guides family screening. Early detection through genetic testing improves patient outcomes by enabling timely and targeted medical interventions.

Why Choose This Immunology Genetic Testing?

Choosing immunology genetic testing offers valuable insights into the genetic basis of immune-related disorders, enabling early diagnosis, accurate risk assessment, and personalized treatment plans. This testing helps identify inherited immune deficiencies, autoimmune conditions, and other immune dysfunctions that might not be detected through standard clinical evaluations. By understanding the root genetic causes, healthcare providers can tailor therapies, avoid unnecessary treatments, and implement proactive care strategies. It is especially beneficial for individuals with recurrent infections, unexplained immune symptoms, or a family history of immune disorders. Ultimately, immunology genetic testing empowers patients and families with knowledge for better health management and decision-making.

When Is It Used?

Recurrent or severe infections – To investigate underlying immune deficiencies.
Early-onset autoimmune diseases – For identifying genetic causes of abnormal immune responses.
Family history of immune disorders – To assess inherited risks and guide family screening.
Unexplained inflammatory symptoms – When traditional tests fail to provide a clear diagnosis.
Before immunosuppressive therapy – To evaluate genetic risks and optimize treatment strategies.
Persistent allergy-like symptoms – To explore potential immunogenetic conditions.
Bone marrow or organ transplant planning – To ensure genetic compatibility and reduce rejection risks.

Who Should Consider Immunology Genetic Testing?

Immunology genetic testing is recommended for individuals with signs of immune system dysfunction, a personal or family history of immune-related diseases, or unexplained symptoms suggestive of an immune disorder. It is especially useful for patients with early-onset or chronic autoimmune conditions, repeated infections, or those who are unresponsive to standard treatments. This testing also benefits individuals preparing for organ or bone marrow transplants and those with relatives already diagnosed with a known genetic immune condition. By identifying genetic mutations affecting immune function, this test can guide clinical decisions and help manage risks for both patients and family members.

You should consider this test if:

Individuals with recurrent, severe, or unusual infections Patients with early-onset or multiple autoimmune diseases
People with a family history of immunodeficiency or autoimmunity
Children with failure to thrive or developmental delays linked to immune dysfunction
Individuals with chronic inflammation or unexplained immune-related symptoms
Candidates for bone marrow or organ transplantation Relatives of patients with a known immunogenetic disorder

How We Work

How is the Test Performed?

Our Services

Just a few of the many health issues we screen for

Severe Combined Immunodeficiency

A rare genetic disorder causing profound immune system failure, leading to life-threatening infections early in infancy.

Common Variable Immunodeficiency

A disorder with low antibody levels, causing frequent bacterial infections and increased risk of autoimmune diseases or lymphomas.

Chronic Granulomatous Disease

A condition where white blood cells fail to kill certain bacteria and fungi, leading to severe, recurring infections.

Wiskott-Aldrich Syndrome

A rare X-linked disorder involving low platelet count, eczema, and increased susceptibility to infections and autoimmune complications.

DiGeorge Syndrome (22q11.2 deletion)

A genetic condition causing immune deficiency, heart defects, learning problems, and facial abnormalities from thymic hypoplasia.

Interferon Gamma Receptor Deficiency

A rare condition causing vulnerability to mycobacterial infections due to defective immune signaling pathways.

Who we Are

Why Choose Us?

State-of-the-Art Digital Lab Experience

Our fully integrated E-Lab platform offers online test ordering, real-time tracking, and secure digital reporting bringing convenience and control to both physicians and patients across the country.

Advanced Diagnostic Technology

From routine blood tests to complex genetic panels, we leverage cutting-edge platforms like NGS, PCR, and AI-powered analytics for maximum accuracy and clinical relevance.

Fast Turnaround, Local Support

With lab facilities based in Florida, we ensure faster processing times and direct access to our expert team. You get timely results backed by responsive, local customer support.

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Comprehensive Thyroid Panel
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Food Sensitivity & Allergy Testing (IgG/IgE Panels)
STI/STD Comprehensive Panel (PCR or Blood Tests)
Diabetes Panel (HbA1c, Fasting Glucose, Insulin, C-Peptide)
Autoimmune Disease Panel

TESTS

NGS TESTING

PCR TESTING

Infectious Disease