Nonspherocytic haemolytic anaemia due to hexokinase deficiency (Q99644): Difference between revisions
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Revision as of 16:19, 16 August 2026
Nonspherocytic haemolytic anaemia due to hexokinase deficiency is characterised by severe haemolysis, appearing in infancy. Seventeen affected families have been reported so far. Transmission is autosomal recessive. Mutations have been described in HK1, the gene that encodes red blood cell-specific hexokinase-R.
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| default for all languages | ID_1942043262 |
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| English | Nonspherocytic haemolytic anaemia due to hexokinase deficiency |
Nonspherocytic haemolytic anaemia due to hexokinase deficiency is characterised by severe haemolysis, appearing in infancy. Seventeen affected families have been reported so far. Transmission is autosomal recessive. Mutations have been described in HK1, the gene that encodes red blood cell-specific hexokinase-R. |
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CID11:ID_1942043262
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