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Dermatology ; 232(2): 129-36, 2016.
Article in English | MEDLINE | ID: mdl-26736030

ABSTRACT

Adamantiades-Behçet disease (ABD) is a chronic, multisystemic, recurrent, inflammatory vascular disorder of unknown etiology. Patients with symptoms initially appearing at the age of 16 or less are considered as cases of juvenile-onset ABD (JABD). JABD is relatively rare compared to ABD of adults, and only case reports and case studies have been published regarding this subtype of the disease. Epidemiology, clinical features, diagnosis and treatment of JABD are discussed in this review.


Subject(s)
Behcet Syndrome/complications , Behcet Syndrome/diagnosis , Adolescent , Arthralgia/etiology , Behcet Syndrome/drug therapy , Behcet Syndrome/epidemiology , Child , Eye Diseases/etiology , Humans , Infant, Newborn , Intestinal Diseases/etiology , Nervous System Diseases/etiology , Vascular Diseases/etiology
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