Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children - a case report with a review

• Main Authors: Jayesh Sheth (Author), Akash Patel (Author), Raju Shah (Author), Riddhi Bhavsar (Author), Sunil Trivedi (Author), Frenny Sheth (Author)
• Formato: Livro
• Publicado em: BMC, 2019-03-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

Abstract Background Hemophagocytic Lymphohistiocytosis (HLH) is a rare, complex, life-threatening hyper-inflammatory condition due to over activation of lymphocytes mediated secretory cytokines in the body. It occurs as a primary HLH due to genetic defect that mostly occurs in the childhood and asso...