Atransferrinemia
Atransferrinemia, also called familial hypotransferrinemia, is an autosomal recessive metabolic disorder in which there is an absence of transferrin, a plasma protein that transports iron through the blood. Atransferrinemia is characterized by anemia and hemosiderosis in the heart and liver. The iron damage to the heart can lead to heart failure. The anemia is typically microcytic and hypochromic (the red blood cells are abnormally small and pale). Atransferrinemia is extremely rare, with only eight cases documented worldwide.
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Atransferrinemia
Atransferrinemia, also called familial hypotransferrinemia, is an autosomal recessive metabolic disorder in which there is an absence of transferrin, a plasma protein that transports iron through the blood. Atransferrinemia is characterized by anemia and hemosiderosis in the heart and liver. The iron damage to the heart can lead to heart failure. The anemia is typically microcytic and hypochromic (the red blood cells are abnormally small and pale). Atransferrinemia is extremely rare, with only eight cases documented worldwide.
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Atransferrinemia, also called ...... ht cases documented worldwide.
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Die hereditäre oder kongenital ...... isenüberladung (Hämosiderose).
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721,912,462
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Violet, a 2-year-old European girl with atransferrinemia.
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Atransferrinemia, also called ...... ht cases documented worldwide.
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Die hereditäre oder kongenital ...... rd autosomal rezessiv vererbt.
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Atransferrinemia
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Hereditäre Atransferrinämie
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Atransferrinemia
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