Hereditary persistence of fetal haemoglobin - sickle cell disease (Q59821): Difference between revisions
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Esta é uma condição benigna na qual produção significativa de hemoglobina fetal (hemoglobina F) continua até a idade adulta, desconsiderando o ponto de encerramento normal na qual apenas o tipo adulto da hemoglobina deveria ser produzido. Este diagnóstico é feito com doença falciforme. | |||
| description / en | description / en | ||
This is a benign condition in which significant fetal haemoglobin (haemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult-type haemoglobin should be produced. This diagnosis is with sickle cell disease. | |||
Revision as of 07:20, 14 August 2026
This is a benign condition in which significant fetal haemoglobin (haemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult-type haemoglobin should be produced. This diagnosis is with sickle cell disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1455152722 |
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| English | Hereditary persistence of fetal haemoglobin - sickle cell disease |
This is a benign condition in which significant fetal haemoglobin (haemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult-type haemoglobin should be produced. This diagnosis is with sickle cell disease. |
