Susceptibility to respiratory infections associated with CD8alpha chain mutation

Orpha code: 169085OMIM code: 608957

Definition

A rare primary immunodeficiency due to a defect in adaptive immunity characterized by the absence of CD8+ T cells with normal immunoglobulin and specific antibody titres in blood and susceptibility to recurrent respiratory bacterial and viral infections. Symptom severity range from fatal respiratory insufficiency to mild or asymptomatic phenotypes.

Disease data
Classification

Disease

Synonyms
Familial CD8 deficiency
Rodzinny Niedobór CD8
ORPHA code
169085
OMIM code
608957
ICD10 code
D84.8
ICD11 code
4A01.1Y

No additional description.

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