Park C L, Streicher H, Rothberg R
J Clin Microbiol. 1987 Jun;25(6):1119-21. doi: 10.1128/jcm.25.6.1119-1121.1987.
The acquired immunodeficiency syndrome-related complex was identified in a mother and one of her nonidentical twins. Generalized lymphadenopathy was first noted in the infant at age 17 months, and that of the mother was incidentally discovered 6 months later. The father, who had had homosexual contacts before the conception of the twins, appeared to be in good health. No one in the family had constitutional symptoms or showed signs of opportunistic infection. Both parents and the patient had hypergammaglobulinemia, low T-helper-to-suppressor-cell ratio, and positive serum antibody to human immunodeficiency virus. Attempts to isolate the virus from all family members were unsuccessful. The twin brother was in good health with a normal immunologic profile and negative antibody to human immunodeficiency virus.
在一位母亲及其非同卵双胞胎之一中发现了与获得性免疫缺陷综合征相关的综合征。该婴儿在17个月大时首次被发现有全身性淋巴结病,6个月后其母亲的全身性淋巴结病被偶然发现。双胞胎受孕前有同性恋接触史的父亲似乎健康状况良好。家中无人有体质性症状或机会性感染迹象。父母及患者均有高球蛋白血症、低辅助性T细胞与抑制性T细胞比例以及抗人类免疫缺陷病毒血清抗体阳性。从所有家庭成员中分离病毒的尝试均未成功。双胞胎中的哥哥健康状况良好,免疫状况正常且抗人类免疫缺陷病毒抗体阴性。