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TFR1 deficiency

Related gene: TFRC

Inheritance pattern: Autosomal recessive

Deficiency of transferrin receptor 1 (TFR1) is a rare, recessive immunodeficiency that has been associated with hypogammaglobulinemia, defective T cell function despite normal quantities, intermittent neutropenia and thrombocytopenia, and mild anemia. TFR1 deficiency has been successfully treated via hematopoietic stem cell transplantation (HSCT) with a resolution of all abnormalities.

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Learn more about combined immune deficiencies.

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Adapted from the IDF Patient & Family Handbook for Primary Immunodeficiency Diseases, Sixth Edition 
Copyright ©2019 by Immune Deficiency Foundation, USA