HLA antigen familial study in complete Behcet's syndrome affecting three sisters

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Abstract

Behcet's disease is a multisystemic disease affecting most organs. Although a tendency towards an association with a certain genetic type and with HLA-B51 is suspected, the incidence of several siblings with Behcet's disease in a single family is rare. A family, in which three sisters were affected with Behcet's disease, uveitis being the most severe manifestation, was studied. In this family all siblings were B51 positive. Only the female siblings, however, with a positive identical HLA phenotype: A2, A11, B51, B44, Cw6, Cw5, DR4, DRw13, DRw53, DRw52, DQw7, DQw6, developed the disease symptoms, whereas none of the male siblings was affected.

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Villanueva, J. L., Gonzalez-Dominguez, J., Gonzalez-Fernandez, R., Prada, J. L., Pena, J., & Solana, R. (1993). HLA antigen familial study in complete Behcet’s syndrome affecting three sisters. Annals of the Rheumatic Diseases, 52(2), 155–157. https://doi.org/10.1136/ard.52.2.155

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