Whether hypogammaglobulinemia is considered a serious disease should be decided according to the patient’s own condition, which can be divided into physiological and pathological, physiological can recover by itself, and pathological needs to be judged according to the cause of the disease.
1. Physiological hypogammaglobulinemia: mostly seen in infants and young children 3~6 months after birth, it is a transient hypogammaglobulinemia and can be recovered by itself.
2. Pathological hypogammaglobulinemia: mostly seen in infants and children, its onset is related to heredity, leukemia, kidney disease and other diseases. If it is a congenital disease, early detection and treatment may have a better prognosis. If hypogammaglobulinemia is caused by heredity, genetic defects, or is secondary, it may be more difficult to treat and may lead to death from infectious shock.
If hypogammaglobulinemia is detected, it is recommended to go to the hospital as soon as possible to identify the cause of the disease and get prompt treatment to avoid delaying the condition.