Złożony Niedobór odporności z powodu deficytu CD3gamma

Kod Orpha: 169082Kod OMIM: 615607

Definicja

A rare autosomal recessive primary immunodeficiency characterized by partial T lymphopenia (in particular cytotoxic CD8+ cells) and decreased expression of the T cell receptor (TCR)/CD3 complex with impaired proliferative response to TCR-dependent stimuli, while the mature memory T cell pool is comparatively well preserved, and B cells, natural killer cells, and immunoglobulins are typically normal. The clinical phenotype is highly heterogeneous, ranging from asymptomatic to infancy-onset of severe recurrent infections, as well as occurrence of autoimmune disease or enteropathy.

Dane
Klasyfikacja

Choroba

Kod ORPHA
169082
Kod OMIM
615607
Kod ICD10
D81.2
Kod ICD11
4A01.1Y

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