RT Book, Section
A1 Hellmann, David B.
A2 Imboden, John B.
A2 Hellmann, David B.
A2 Stone, John H.
SR Print(0)
ID 57273566
T1 Chapter 38. Behçet Disease
T2 CURRENT Diagnosis & Treatment: Rheumatology, 3e
YR 2013
FD 2013
PB The McGraw-Hill Companies
PP New York, NY
SN 978-0-07-163805-0
LK accessmedicine.mhmedical.com/content.aspx?aid=57273566
RD 2023/03/21
AB Recurrent  attacks  of  oral  aphthous  ulcers,  genital  ulcers,  uveitis,  and  skin  lesions.Onset  usually  in  young  adults,  aged  25–35  years.Prevalent  in  parts  of  Asia  and  Europe;  rare  in  North  America.Blindness,  central  nervous  system  disease,  and  large-vessel  events  are  the  most  serious  complications.Glucocorticoids,  immunosuppressive  drugs,  or  both  are  required  for  severe  disease.