Ersoy F, Sanal O, Tezcan I, Berkel A I
Immunology Unit, Hacettepe University Institute of Child Health, Ankara, Turkey.
Turk J Pediatr. 1990 Oct-Dec;32(4):241-7.
The clinical and immunologic features of six patients with X-linked agammaglobulinemia (XLA) are presented. The most common presenting manifestations were respiratory and gastrointestinal tract infections. On admittance to the hospital, one patient had a history of recurrent meningitis, another had a dermatomyositis-like syndrome, and still another had a history of recurrent arthritis.
本文报告了6例X连锁无丙种球蛋白血症（XLA）患者的临床和免疫学特征。最常见的首发表现是呼吸道和胃肠道感染。入院时，1例患者有复发性脑膜炎病史，另1例有皮肌炎样综合征，还有1例有复发性关节炎病史。
