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 / endescription / 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.
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Property / Canonical URI: https://id.who.int/icd/entity/2063292324 / rank
 
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CID11:3A50.2
Property / CURIE: CID11:3A50.2 / rank
 
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dki-india-3A50.2
Property / Canary Token: dki-india-3A50.2 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10: D56.1 / rank
 
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Latest 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.
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3A50.2
    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.

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      CID11:3A50.2
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      dki-india-3A50.2
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      Concluído
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      13 August 2026
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