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原发性体液免疫缺陷病是原发性免疫缺陷病中常见的一类疾病,其并发症严重威胁患儿健康。近年来,原发性体液免疫缺陷病逐渐受到医学界的重视,对原发性体液免疫缺陷病的研究取得了一些重要进展,特别是遗传学及分子生物学方面。研究原发性体液免疫缺陷病的基因情况,对指导临床的诊断、治疗均有积极意义。
Primary humoral immune deficiency disease is a common type of disease in primary immune deficiency disease, its serious threat to children’s health complications. In recent years, the primary humoral immunodeficiency disease gradually by the medical community’s attention, the study of primary humoral immune deficiency made some important progress, especially in genetics and molecular biology. To study the gene status of primary humoral immunodeficiency disease has positive significance in guiding clinical diagnosis and treatment.