Atransferrinemia

Congenital atransferrinemia is a very rare hematologic disease caused by a transferrin (TF) deficiency and characterized by microcytic, hypochromic anemia (manifesting with pallor, fatigue and growth retardation) and iron overload, and that can be fatal if left untreated.

Also known as: atransferrinemia, congenital atransferrinemia, congenital hypotransferrinemia, familial hypotransferrinemia, hereditary atransferrinemia, hypotransferrinemia, familial, transferrin serum level quantitative trait locus 1

64 clinical trials for this condition and its sub-types.