Złożony niedobór odporności z powodu deficytu ITK

Kod Orpha: 538963Kod OMIM: 613011

Definicja

A rare autosomal recessive primary immunodeficiency characterized by susceptibility to Epstein-Barr virus (EBV)-associated lymphoproliferative disorders such as malignant B-cell proliferation, Hodgkin lymphoma, B-cell lymphoma, lymphoid granulomatosis, hemophagocytic lymphohistiocytosis, and smooth muscle tumor. Patients present persistent symptoms of infectious mononucleosis including recurrent febrile episodes, lymphadenopathies, and hepatosplenomegaly, accompanied by high EBV viral load in the blood. Additional manifestations are autoimmune diseases like hemolytic anemia or renal disease.

Dane
Klasyfikacja

Choroba

Synonimy
Autosomal recessive lymphoproliferative disease due to ITK deficiency
Autosomal recessive lymphoproliferative disease due to ITK deficiency
ITK deficiency
Kod ORPHA
538963
Kod OMIM
613011
Kod ICD10
D82.3
Kod ICD11
-

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