Runge L A, Davey F R, Goldberg J, Boyd P R
J Rheumatol. 1986 Feb;13(1):39-42.
A family in which 3 siblings had Felty's syndrome is described. All affected family members shared the common haplotype HLA-A2, B15, Cw3 and DR4. In addition, all affected siblings possessed the A2 and ABO phenotype. Four unaffected siblings possessed either the HLA-A2, B15, Cw3 and DR4 haplotype or the A2 ABO phenotype or neither but not both. We believe our data support the hypothesis that multiple genetic factors are involved in the predisposition of family members to Felty's syndrome.
本文描述了一个有3名兄弟姐妹患费尔蒂综合征的家庭。所有患病家庭成员都具有共同的单倍型HLA - A2、B15、Cw3和DR4。此外,所有患病的兄弟姐妹都具有A2和ABO血型表型。4名未患病的兄弟姐妹要么具有HLA - A2、B15、Cw3和DR4单倍型,要么具有A2 ABO血型表型,要么两者都不具有,但不会同时具备两者。我们认为我们的数据支持这样的假设,即多种遗传因素参与了家庭成员患费尔蒂综合征的易感性。