Bird T D
Arch Neurol. 1975 Jun;32(6):414-6. doi: 10.1001/archneur.1975.00490480080009.
Three members of an unusual family were affected with apparent multiple sclerosis in a direct line over three successive generations. Each affected member had clinical remissions and exacerbations and evidence of lesions disseminated in space. One affected member had a cerebrospinal fluid pleocytosis and elevated gamma-globulin level. The genetically determined histocompatibility antigen (HL-A) types are reported for 13 family members. The three affected members had HL-A types 11 and W16 in common.
一个非同寻常的家族中有三名成员在连续三代中直系亲属都患有明显的多发性硬化症。每一位患病成员都有临床缓解期和加重期,且有病变在空间上播散的证据。一名患病成员脑脊液有细胞增多现象,γ球蛋白水平升高。报告了13名家族成员的基因决定的组织相容性抗原(HL - A)类型。三名患病成员都有共同的HL - A类型11和W16。