No Family Clustering in
Behcet's Syndrome. Balkan Med J 2019;36:145-6
Reynolds, "Vasculitis in
Behcet's syndrome: evidence-based review," Current Opinion in Rheumatology, vol.
Urologicscreening for men with
Behcet's syndrome. Urology 1998; 52: 863-5.
Chamberlain, "
Behcet's syndrome in 32 patients in Yorkshire," Annals of the Rheumatic Diseases, vol.
Beales, "Gastrointestinal involvement in
Behcet's syndrome," American Journal of Gastroenterology, vol.
One year in review 2016:
Behcet's syndrome. Clin Exp Rheumatol.
(4.) Dalvi SR, Yildirim R, Yazici Y
Behcet's Syndrome. Drugs.
Serum leptin concentration is increased in patients with
Behcet's syndrome and is correlated with disease activity.
Behcet's Disease, sometimes called
Behcet's syndrome, or Morbus Behcet, Behcet-Adamantiades syndrome, or Silk Road disease, is a rare immune-mediated small-vessel systemic vasculitis that often presents with mucous membrane ulceration and ocular problems.
Rarely, recurrent mouth ulcers may be due to anaemia, a deficiency of either vitamin B or folic acid, an intestinal disorder, such as Crohn's disease, coeliac disease, or
Behcet's syndrome, a rare autoimmune disorder.
M-mod, 2-D and Doppler echocardiographic study in 65 patient with
Behcet's syndrome. Eur Heart J 1992; 13:638-641.
Results Out of a total of 30 patients diagnosed histologically as cutaneous vasculitis 22 were classified as cutaneous small vessel vasculitis (CSVV) 6 as Heinoch-Schonlein purpura and one each as urticarial vasculitis and
Behcet's syndrome. Approximately 30% of the patients had a significant drug history 23.3% were attributed to infection.