Behcet’s Disease: A Rare Case Report
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Abstract
Behcet’s disease or Behcet’s syndrome is a rare form of vasculitis that can cause symptoms in the oral cavity, skin, eyes, genitals and may also present with other forms of systemic manifestations. This condition is characterised by recurrent aphthous ulcers in the oral mucosa, acneform eruptions on the skin, anterior or posterior uveitis and genital ulcers [1].
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