Individuals with immunodeficiency following hereditary defective response to EBV have a genetic mutation that affects their immune system's ability to fight off the virus. As a result, they may experience frequent and severe infections, including EBV-associated lymphomas and other cancers.
EBV is a member of the herpesvirus family and can cause infectious mononucleosis, also known as "mono." While most people recover from mono without complications, individuals with immunodeficiency following hereditary defective response to EBV may experience chronic EBV infection and an increased risk of developing lymphoma.
There are several types of immunodeficiency following hereditary defective response to EBV, including X-linked lymphoproliferative syndrome (XLP), which primarily affects males, and other less common genetic mutations that affect both males and females.
Diagnosis of immunodeficiency following hereditary defective response to EBV typically involves a combination of clinical evaluation, blood tests, and genetic testing to identify the specific genetic mutation affecting the immune system.
While there is no cure for immunodeficiency following hereditary defective response to EBV, treatment typically involves managing symptoms and preventing or treating infections as they arise. This may include antiviral medications, immunoglobulin replacement therapy, and other supportive measures to boost the immune system's response to infections.
Individuals with immunodeficiency following hereditary defective response to EBV should work closely with their healthcare provider to manage their symptoms and reduce their risk of developing complications from chronic EBV infection.
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