Abstract: | Tissue typing was performed on lymphocytes of
74 unrelated patients and 12 families with multiple
affected siblings. HLA-B13, Aw19, B17 (Bw57),
Cwl, DRl were found increased. The analysis of
haplotype showed that one or two haplotype sharing
among affected siblings occurred more frequently
than expected (p<0.0001). The result of lods score
for 4 families was l.940. These findings suggest that
there may be at least one disease gene linked with
MHC involved in this disease. |