Beta thalassaemia associated with other haemoglobin anomaly (Q51366): Difference between revisions
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A talassemia beta associada a anomalias da hemoglobina (Hb) resulta em um espectro clínico amplo, variando de assintomático a grave, dependendo da gravidade da mutação da talassemia e do tipo de anomalia da Hb [persistência hereditária da Hb fetal, talassemia delta-beta, Hb C - talassemia beta, Hb E - talassemia beta e Hb S - talassemia beta]. | |||
| description / en | description / en | ||
Beta-thalassemias associated with haemoglobin (Hb) anomalies result in a variable clinical spectrum, ranging from asymptomatic to severe, depending on the severity of the thalassemia mutation and on the type of the Hb anomaly [hereditary persistence of fetal Hb, delta-beta-thalassemia, Hb C - beta-thalassemia, Hb E - beta-thalassemia and Hb S - beta-thalassemia]. | |||
Revision as of 22:32, 13 August 2026
Beta-thalassemias associated with haemoglobin (Hb) anomalies result in a variable clinical spectrum, ranging from asymptomatic to severe, depending on the severity of the thalassemia mutation and on the type of the Hb anomaly [hereditary persistence of fetal Hb, delta-beta-thalassemia, Hb C - beta-thalassemia, Hb E - beta-thalassemia and Hb S - beta-thalassemia].
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2056576450 |
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| English | Beta thalassaemia associated with other haemoglobin anomaly |
Beta-thalassemias associated with haemoglobin (Hb) anomalies result in a variable clinical spectrum, ranging from asymptomatic to severe, depending on the severity of the thalassemia mutation and on the type of the Hb anomaly [hereditary persistence of fetal Hb, delta-beta-thalassemia, Hb C - beta-thalassemia, Hb E - beta-thalassemia and Hb S - beta-thalassemia]. |
