» Articles » PMID: 23179819

[Behçet's Disease - Ophthalmological and General Aspects Part I : Etiology, Pathogenesis and Diagnostics]

Overview
Journal Ophthalmologe
Specialty Ophthalmology
Date 2012 Nov 27
PMID 23179819
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Behçet's disease (also known as morbus Behcet or Admantiades-Behcet syndrome) is a chronic vasculitis mainly characterized by recurrent mucocutaneous lesions and sight threatening uveitis. It may also involve joints, vessels of all sizes and the central nervous system. Because of its severe morbidity and considerable mortality early diagnosis and treatment is important. Treatment and prognosis of this disorder have profited considerably in recent years following the introduction of biologic agents. This article summarizes the current state of knowledge and emphasizes the important role of the ophthalmologist in the diagnosis and therapy of Behçet's disease.

Citing Articles

Bilateral Retrobulbar Optic Neuritis as the First Manifestation of Neuro-Behçet Disease.

Jari M, Mohammadi T, Taheri E Case Rep Rheumatol. 2020; 2020:8834399.

PMID: 33083081 PMC: 7559221. DOI: 10.1155/2020/8834399.


Neuropsychiatric and behavioral profiles of 2 adults with williams syndrome: response to antidepressant intake.

Urgeles D, Alonso V, Ramos-Moreno T Prim Care Companion CNS Disord. 2014; 15(4).

PMID: 24392262 PMC: 3869614. DOI: 10.4088/PCC.13m01504.


Behcet's disease: systemic and ocular manifestations.

Paovic J, Paovic P, Sredovic V Biomed Res Int. 2013; 2013:247345.

PMID: 24199188 PMC: 3808725. DOI: 10.1155/2013/247345.


Correlation between Ocular Manifestations and Their Complications as Opposed to Visual Acuity and Treatment in Behcet's Disease.

Paovic J, Paovic P, Sredovic V Autoimmune Dis. 2013; 2013:842673.

PMID: 24073331 PMC: 3773399. DOI: 10.1155/2013/842673.


[Behcet's disease--ophthalmological and general aspects: Part 2: Therapy].

Pleyer U, Hazirolan D, Winterhalter S, Stubiger N Ophthalmologe. 2013; 110(3):273-84.

PMID: 23504099 DOI: 10.1007/s00347-012-2780-z.

References
1.
Deuter C, Kotter I, Wallace G, Murray P, Stubiger N, Zierhut M . Behçet's disease: ocular effects and treatment. Prog Retin Eye Res. 2007; 27(1):111-36. DOI: 10.1016/j.preteyeres.2007.09.002. View

2.
Ozturk M, Ertenli I, Kiraz S, Haznedaroglu I, Celik I, Kirazli S . Plasminogen activator inhibitor-1 as a link between pathological fibrinolysis and arthritis of Behçet's disease. Rheumatol Int. 2003; 24(2):98-102. DOI: 10.1007/s00296-003-0324-1. View

3.
Hazirolan D, Sungur G, Duman S . Demographic, clinical, and ocular features in patients with late-onset Behçet disease. Ocul Immunol Inflamm. 2012; 20(2):119-24. DOI: 10.3109/09273948.2012.655882. View

4.
Altenburg A, Papoutsis N, Orawa H, Martus P, Krause L, Zouboulis C . [Epidemiology and clinical manifestations of Adamantiades-Behçet disease in Germany -- current pathogenetic concepts and therapeutic possibilities]. J Dtsch Dermatol Ges. 2006; 4(1):49-64. DOI: 10.1111/j.1610-0387.2006.05841.x. View

5.
Chajek-Shaul T, Pisanty S, Knobler H, Matzner Y, Glick M, Ron N . HLA-B51 may serve as an immunogenetic marker for a subgroup of patients with Behçet's syndrome. Am J Med. 1987; 83(4):666-72. DOI: 10.1016/0002-9343(87)90896-5. View