Beta thalassaemia (Q39517): Difference between revisions
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A talassemia beta (BT) é uma hemoglobinopatia caracterizada por deficiência (Beta+) ou ausência (Beta0) da síntese das cadeias de beta globina da hemoglobina (Hb). Foram descritos três tipos principais da BT: menor, intermédia e maior com apresentação clínica variando de formas assintomáticas a anemia microcítica e esplenomegalia devido a eritropoiese defeituosa e hemólise. | |||
| description / en | description / en | ||
Beta-thalassemia (BT) is a haemoglobinopathy characterised by deficiency (Beta+) or absence (Beta0) of synthesis of the beta globin chains of haemoglobin (Hb). Three main types of BT have been described: minor, intermedia and major with clinical presentation ranging from asymptomatic forms to microcytic anaemia and splenomegaly due to defective erythropoiesis and haemolysis. | |||
Revision as of 04:57, 13 August 2026
Beta-thalassemia (BT) is a haemoglobinopathy characterised by deficiency (Beta+) or absence (Beta0) of synthesis of the beta globin chains of haemoglobin (Hb). Three main types of BT have been described: minor, intermedia and major with clinical presentation ranging from asymptomatic forms to microcytic anaemia and splenomegaly due to defective erythropoiesis and haemolysis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A50.2 |
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| English | Beta thalassaemia |
Beta-thalassemia (BT) is a haemoglobinopathy characterised by deficiency (Beta+) or absence (Beta0) of synthesis of the beta globin chains of haemoglobin (Hb). Three main types of BT have been described: minor, intermedia and major with clinical presentation ranging from asymptomatic forms to microcytic anaemia and splenomegaly due to defective erythropoiesis and haemolysis. |
