Haemolytic anaemias due to hexose monophosphate shunt or glutathione metabolism anomalies (Q39507): Difference between revisions

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Esta doença é um tipo de anemia devido a hemólise, destruição anormal dos glóbulos vermelhos ( hemácias ), tanto nos vasos sanguíneos (hemólise intravascular) ou em outro local no organismo humano ( extravascular ). Este diagnóstico se deve a um processo que gera NADPH e pentoses ( açúcares de 5 carbonos ) e anormalidades no metabolismo da glutationa.
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This is a form of anaemia due to haemolysis, the abnormal breakdown of red blood cells (RBCs), either in the blood vessels (intravascular haemolysis) or elsewhere in the human body (extravascular). This diagnosis is due to a process that generates NADPH and pentoses (5-carbon sugars) and glutathione metabolism anomalies.

Revision as of 04:57, 13 August 2026

This is a form of anaemia due to haemolysis, the abnormal breakdown of red blood cells (RBCs), either in the blood vessels (intravascular haemolysis) or elsewhere in the human body (extravascular). This diagnosis is due to a process that generates NADPH and pentoses (5-carbon sugars) and glutathione metabolism anomalies.
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3A10.0
    English
    Haemolytic anaemias due to hexose monophosphate shunt or glutathione metabolism anomalies
    This is a form of anaemia due to haemolysis, the abnormal breakdown of red blood cells (RBCs), either in the blood vessels (intravascular haemolysis) or elsewhere in the human body (extravascular). This diagnosis is due to a process that generates NADPH and pentoses (5-carbon sugars) and glutathione metabolism anomalies.

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