Blau syndrome: A case report of a rare granulomatous disorder

• मुख्य लेखकों: Preema Sinha (लेखक), S Kartik (लेखक), Jasvinder Kaur Bhatia (लेखक), Thrinley Choden (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Wolters Kluwer Medknow Publications, 2020-01-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: 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...