Hereditary persistence of fetal haemoglobin (Q39520): Difference between revisions
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A persistência hereditária da hemoglobina fetal (HPFH) associada com a beta talassemia é uma hemoglobinopatia caracterizada pelos níveis elevados de hemoglobina (Hb) F e um número aumentado de células contendo Hb fetal. A associação da HPFH com beta talassemia atenua as manifestações clínicas as quais variam de um estado normal a beta talassemia intermédia. | |||
| description / en | description / en | ||
Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia. | |||
Revision as of 04:58, 13 August 2026
Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A50.4 |
||
| English | Hereditary persistence of fetal haemoglobin |
Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia. |
