X-linked lymphoproliferative disease due to SH2D1A deficiency

MONDO:0024551

A rare, genetic, primary immunodeficiency disorder characterized by an abnormal immune response to Epstein-Barr virus (EBV) infection, caused by hemizygous mutations in the X-linked SH2D1A gene, resulting in B cell lymphoproliferation and manifesting with various phenotypes which include EBV-driven severe or fulminant mononucleosis, hemophagocytic lymphohistiocytosis (presenting with fulminant hepatitis, hepatic necrosis, bone marrow hypoplasia, and neurological involvement), hypogammaglobulinemia, and B-cell lymphoma. Additional variable manifestations include vasculitis, lymphomatoid granulomatosis, aplastic anemia, and chronic gastritis. Occasionally, T-cell lymphoma may be observed. Laboratory findings include normal or increased activated T cells and reduced memory B cells.

Also known as: X-linked lymphoproliferative disease due to SH2D1A deficiency, lymphoproliferative syndrome, X-linked, 1, X-linked recessive, Duncan disease, EBV infection, Severe, susceptibility to, Epstein-Barr Virus infection, familial fatal, Lyp, Purtilo syndrome, XLP1

61 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by