Ming Jeffrey E, Stiehm E Richard
Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, The University of Pennsylvania School of Medicine, 3615 Civic Center Boulevard, Philadelphia, PA 19104, USA.
Immunol Allergy Clin North Am. 2008 Nov;28(4):715-36, vii. doi: 10.1016/j.iac.2008.06.007.
This article reviews the major syndromic immunodeficiencies with significant antibody defects, many of which may require intravenous immunogammaglobulin therapy. The authors define syndromic immunodeficiency as an illness associated with a characteristic group of phenotypic abnormalities or laboratory features that comprise a recognizable syndrome. Many are familial with a defined inheritance pattern. Immunodeficiency may not be a major part of the illness and may not be present in all patients; thus, these conditions differ from primary immunodeficiency syndromes, in which immune abnormalities are a consistent and prominent feature of their disease.
本文综述了伴有显著抗体缺陷的主要综合征性免疫缺陷病,其中许多可能需要静脉注射免疫球蛋白治疗。作者将综合征性免疫缺陷定义为一种与一组特征性表型异常或实验室特征相关的疾病,这些异常或特征构成了一种可识别的综合征。许多病例为家族性,具有明确的遗传模式。免疫缺陷可能不是疾病的主要部分,也并非在所有患者中都存在;因此,这些病症与原发性免疫缺陷综合征不同,后者的免疫异常是其疾病始终存在且突出的特征。