An individual with primary immunodeficiency is highly prone to infections, autoimmunity, autoinflammatory diseases, and allergies because of genetic factors. A spectrum of inborn immune errors has been discovered in recent years, expanding our understanding from simply immune defects.
Using the Comprehensive Primary Immunodeficiency NGS Panel, you can diagnose and treat a variety of conditions associated with immunodeficiency.

It is recommended for individuals with frequent infections, fevers, allergies, malignancies, or rashes, especially if those infections are severe or recurrent. Accurate diagnosis, treatment guidance, lifestyle adjustments, personalized care, risk assessment, support resources, and family planning options are among the benefits.

Who should consider this test?

Those with a personal or family history of infections, fevers, allergies, certain malignancies, or rash, especially infections that are recurrent, difficult to treat, require hospitalization or IV antibiotics, or are caused by uncommon organisms.

How can your patient benefit from it?

Diagnostic confirmation and treatment guidance for patients with immunodeficiency, enabling them to take preventive measures against infections. Genetic testing helps to develop a management plan by:

• Providing guidance on reproductive choices and family planning.

• Informing relatives about potential health risks related to the condition.

• Linking patients to helpful support groups and resources.

• Recommending lifestyle changes to improve health and manage symptoms.

• Identifying risks for complications or additional symptoms.

• Using evaluations and tests to confirm or establish a diagnosis.

• Tailoring treatments to meet the unique needs of each patient.