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Congenital atransferrinemia

Known as: Atransferrinemia, Familial hypotransferrinemia, Hypotransferrinemia, Familial 
An extremely rare iron overload disorder caused by mutation in the structural gene for transferrin (TF gene). It is characterized by hypochromic… 
National Institutes of Health

Related topics

Related topics

2 relations
TF, ALA477PRO

Broader (1)

Transferrin

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
A Rare Case of Congenital Atransferrinemia: International Collaboration for Genetic Diagnosis
Congenital atransferrinemia is an extremely rare hematologic disease caused by transferrin deficiency, and characterized by… 
2005
2005
A Family of Congenital Atransferrinemia Blood
An 8-yr-old boy with familial congenital atransferrinemia was studied. He had marked hypochromic anemia but did not respond to… 
2002
2002
Congenital atransferrinemia: a case report
Objective Congenital atransferrinemia (CAT) is an extremely rarely, recessively inherited disorder. To date, only eight cases… 
1988
1988
Further evidence of a silent Tf allele
Since the detection of transferrin polymorphism by Smithies in the year 1957 some cases of inherited atransferrinemia have been… 
1986
1986
[Iron overload in hereditary atransferrinemia].
1982
1982
[Atransferrinemia secondary to hepatic cirrhosis, hemochromatosis, and nephrotic syndrome].
1982
1982
[Atransferrinemia secondary to hepatic cirrhosis, hemochromatosis, and nephrotic syndrome].
1977
1977
A Case of Atransferrinemia and 35 Cases of Hypotransferrinemia as Detected by Radioassay of Total Iron-binding Capacity of the Serum
1974
1974
[Hereditary atransferrinemia].
1968
1968
[Congenital atransferrinemia in a 11-month-old child].
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