Autoimmune lymphoproliferative syndrome-recurrent viral infections due to CASP8 deficiency
ORPHA:275517· ICD-10 D47.9
Definition
A rare genetic disorder characterized by lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal recessive
- Age of onset
- Childhood