Blau syndrome: A case report of a rare granulomatous disorder

• Main Authors: Preema Sinha (Author), S Kartik (Author), Jasvinder Kaur Bhatia (Author), Thrinley Choden (Author)
• Formato: Libro
• Publicado: Wolters Kluwer Medknow Publications, 2020-01-01T00:00:00Z.
• Subjects: article
• Acceso en liña: Connect to this object online.

Blau syndrome is a rare condition characterized by the triad of granulomatous skin lesions, symmetric polyarthritis with boggy joint swellings, and ocular inflammation. It has an autosomal dominant mode of inheritance and occurs due to a mutation in CARD-15/NOD-2 gene which encodes the cytosolic NOD...