Autoimmune lymphoproliferative syndrome type 2B

Autoimmune lymphoproliferative syndrome (ALPS) with recurrent viral infections is a rare genetic disorder characterized by lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses.

Also known as: ALPS2B, CASP8 autoimmune lymphoproliferative syndrome, CEDS, autoimmune lymphoproliferative syndrome caused by mutation in CASP8, autoimmune lymphoproliferative syndrome, type IIB, caspase 8 deficiency, caspase 8 deficiency syndrome, Ceds

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