HLA antigen familial study in complete Behçet's syndrome affecting three sisters.
Ann Rheum Dis
; 52(2): 155-7, 1993 Feb.
Article
in En
| MEDLINE
| ID: mdl-8447696
Behçet'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 Behçet's disease in a single family is rare. A family, in which three sisters were affected with Behçet'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.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Behcet Syndrome
/
HLA Antigens
Limits:
Adult
/
Female
/
Humans
/
Male
Language:
En
Journal:
Ann Rheum Dis
Year:
1993
Document type:
Article
Affiliation country:
Spain
Country of publication:
United kingdom