I. Pande et al., BEHCETS-DISEASE IN INDIA - A CLINICAL, IMMUNOLOGICAL, IMMUNOGENETIC AND OUTCOME STUDY, British journal of rheumatology, 34(9), 1995, pp. 825-830
The clinical and laboratory profile of 58 consecutive patients satisfy
ing the ISG 1990 criteria for the diagnosis of Behcet's disease was an
alysed. It appears that Behcet's disease in India is predominantly 'mu
cocutaneous' and 'arthritic'; 'ocular' and 'neuro' Behcet's being unco
mmon. In comparison to published literature, the onset of disease in t
his part of the world is significantly delayed. The pathergy test is r
arely positive. There is no significant difference in clinical present
ation and laboratory investigations between children and adults with t
his disease; also, no sex difference was observed. A combination of or
al steroids and colchicine gives good relief in most cases. Preliminar
y observations seem to reflect no definite association of any known cl
ass I antigen to disease in this part of the world. A detailed study o
n immunogenetics is underway.