Robson S C, Potter P C
MRC/UCT Liver Research Center, University of Cape Town, Observatory, South Africa.
J Clin Lab Immunol. 1990 Jul;32(3):143-6.
Common variable immunodeficiency is a heterogeneous syndrome which may occur at any age and may be associated with recurrent sinopulmonary and gastro-intestinal infections, atopic illness, autoimmune disorders and varying degrees of hypogammaglobulinaemia (1). The clinical syndrome is very similar to that described in X-linked agamma-globulinaemia but the mode of inheritance is unknown (2). In this communication, a patient with Turner's syndrome with X-isoX chromosomal pattern in conjunction with common variable immunodeficiency is reported.
普通变异型免疫缺陷是一种异质性综合征，可发生于任何年龄，可能与反复的鼻窦肺部和胃肠道感染、特应性疾病、自身免疫性疾病以及不同程度的低丙种球蛋白血症有关（1）。该临床综合征与X连锁无丙种球蛋白血症中所描述的非常相似，但遗传方式尚不清楚（2）。在本报告中，报道了一名患有特纳综合征且具有X-isoX染色体模式并伴有普通变异型免疫缺陷的患者。
