Alpha thalassaemia (Q39515): Difference between revisions
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A alfa-talassemia é uma hemoglobinopatia hereditária caracterizada pela síntese prejudicada de cadeias da alfa-globina levando a um quadro clinico variável dependendo do número de alelos afetados, e abrangendo o traço alfa-talassêmico, a doença da hemoglobina H (HbH) e a hidropisia fetal de Barts. | |||
| description / en | description / en | ||
Alpha-thalassemia is an inherited haemoglobinopathy characterised by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles, and encompassing the alpha thalassaemia trait, haemoglobin H disease (HbH) and Bart's hydrops fetalis. | |||
Revision as of 04:57, 13 August 2026
Alpha-thalassemia is an inherited haemoglobinopathy characterised by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles, and encompassing the alpha thalassaemia trait, haemoglobin H disease (HbH) and Bart's hydrops fetalis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A50.0 |
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| English | Alpha thalassaemia |
Alpha-thalassemia is an inherited haemoglobinopathy characterised by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles, and encompassing the alpha thalassaemia trait, haemoglobin H disease (HbH) and Bart's hydrops fetalis. |
