primary immunodeficiency

How is Primary Immunodeficiency Diagnosed?


Diagnosis typically involves a combination of clinical evaluation and laboratory tests. Key diagnostic steps include:
Detailed medical history and physical examination
Blood tests to measure levels of immune cells and antibodies
Genetic testing to identify specific gene mutations
Imaging studies such as X-rays or CT scans to assess organ health
Early diagnosis is crucial for effective management and improving the child’s quality of life.

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