Złożony niedobór odporności zależny od TFRC

Kod Orpha: 476113Kod OMIM: 616740

Definicja

A rare genetic combined T and B cell immunodeficiency characterized by life-threatening infections due to disrupted transferrin receptor 1 endocytosis, resulting in defective cellular iron transport and impaired T and B cell function. Patients present with early-onset chronic diarrhea, severe recurrent infections, and failure to thrive. Laboratory studies reveal hypo- or agammaglobulinemia, normal lymphocyte counts but decreased numbers of memory B cells, intermittent neutropenia and thrombocytopenia, and mild anemia (resistant to iron supplementation) with low mean corpuscular volume.

Dane
Klasyfikacja

Choroba

Synonimy
CID due to TFRC deficiency
TFRC-related combined immunodeficiency
CID due to TFRC deficiency
TFRC-related combined immunodeficiency
Kod ORPHA
476113
Kod OMIM
616740
Kod ICD10
D81.8
Kod ICD11
-

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