Alpha thalassaemia myelodysplastic syndrome (Q91736): Difference between revisions
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Talassemia alfa é um tipo de talassemia envolvendo os genes HBA1 e HBA2. A talassemia alfa é devida a produção prejudicada das cadeias da alfa globina 1,2,3 ou 4, levando a um excesso relativo de cadeias da beta globina. A síndrome mielodisplásica é uma coleção diversa de condições médicas hematológicas (relacionadas ao sangue) que envolve produção ineficaz (ou displasia) de células sanguíneas da classe mieloides. | |||
| description / en | description / en | ||
Alpha-thalassemia is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. Myelodysplastic syndrome is a diverse collection of haematological (blood-related) medical conditions that involve ineffective production (or dysplasia) of the myeloid class of blood cells. | |||
Revision as of 18:46, 15 August 2026
Alpha-thalassemia is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. Myelodysplastic syndrome is a diverse collection of haematological (blood-related) medical conditions that involve ineffective production (or dysplasia) of the myeloid class of blood cells.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1991581630 |
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| English | Alpha thalassaemia myelodysplastic syndrome |
Alpha-thalassemia is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains. Myelodysplastic syndrome is a diverse collection of haematological (blood-related) medical conditions that involve ineffective production (or dysplasia) of the myeloid class of blood cells. |
