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[Behcet's disease: a rarely recognized orphan disorder].
- Source :
-
Orvosi hetilap [Orv Hetil] 2013 Jan 20; Vol. 154 (3), pp. 93-101. - Publication Year :
- 2013
-
Abstract
- Behcet's disease is a multisystem autoimmune disease with variable clinial manifestations. The diagnosis may pose a difficult challenge for the clinician, who has to be familiar with the wide spectrum and combination of the symptoms of Behcet's disease. It is considered a rare disease in Hungary, and there are only few reports on Behcet's disease in the Hungarian literature. However, the past history of Hungary, the worldwide growing incidence of the disease, and the authors' experience raise the possibility that the occurrence of the disease is higher than previously thought. In this review the authors present and discuss literature data on the pathogenesis and pathomechanism, as well as their own experience concerning the symptomatology of Behcet's disease in order to promote diagnosis and offer adequate therapy for the patients. The authors presume that the importance of the disease is underestimated in Hungary due to a considerable number of unrecognized cases and they propose to establish a national registry for Behcets disease.
- Subjects :
- Autoimmunity
Cardiovascular System physiopathology
Central Nervous System physiopathology
Diagnosis, Differential
Gastrointestinal Tract physiopathology
Humans
Hungary epidemiology
Incidence
Musculoskeletal System physiopathology
Retinal Vasculitis etiology
Risk Factors
Stomatitis, Aphthous etiology
Behcet Syndrome complications
Behcet Syndrome diagnosis
Behcet Syndrome epidemiology
Behcet Syndrome etiology
Behcet Syndrome physiopathology
Behcet Syndrome therapy
Rare Diseases diagnosis
Subjects
Details
- Language :
- Hungarian
- ISSN :
- 0030-6002
- Volume :
- 154
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Orvosi hetilap
- Publication Type :
- Academic Journal
- Accession number :
- 23315224
- Full Text :
- https://doi.org/10.1556/OH.2013.29528