Microchimerism in Behçet's disease

Background Behçet's disease (BD) is a multisystemic disorder of unknown etiology characterized by chronic relapsing oral aphthous lesions, genital ulcers, and uveitis. Immunological dysfunction is the most emphasized etiopathogenetic factor. Microchimerism is existence of an allogeneic DNA in a...

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Veröffentlicht in:	International journal of dermatology 2014-07, Vol.53 (7), p.832-837
Hauptverfasser:	Alp, Ruken, Guney, Aysequl U., Tursen, Umit, Kaya, Tamer, Tursen, Belma, Erdal, Mehmet E.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Autoimmune Diseases - genetics Behcet Syndrome - genetics Chimerism Female Humans Male Middle Aged Nuclear Family Sex-Determining Region Y Protein - genetics Young Adult
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