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Acute haemolytic anaemia and myolysis due to G6PD deficiency
A 2-year-old African-American male patient with sickle cell trait developed cough, red coloured urine, pallor and fatigue. The patient was hospitalised. Diagnostic workup showed that he was glucose 6 phosphate dehydrogenase (G6PD) deficient in erythrocytes. He also had chest X-ray findings of pneumo...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4170498/ https://ncbi.nlm.nih.gov/pubmed/25234071 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2014-203631 |
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