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T-cell immunodeficiency with epidermodysplasia verruciformis

ORPHA:324294· ICD-10 D84.8

Definition

A rare primary immunodeficiency characterized by increased susceptibility to infection by human papillomavirus, presenting in childhood with disseminated flat wart-like cutaneous lesions. Burkitt lymphoma has also been reported. Whilst total T-cell counts are normal, there is impaired TCR signaling, profound peripheral naive T-cell lymphopenia with memory T-cells displaying an exhaustion phenotype.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal recessive
Age of onset
Childhood