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Gilbert’s syndrome coexisting with hereditary spherocytosis might not be rare: Six case reports
BACKGROUND: Both Gilbert's syndrome (GS) and hereditary spherocytosis (HS) are common genetic disorders. However, comorbidity of GS with HS has always been considered a rare phenomenon, and it can impede accurate diagnoses in the presence of isolated unconjugated hyperbilirubinemia. CASE SUMMAR...
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| Опубликовано в: : | World J Clin Cases |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Baishideng Publishing Group Inc
2020
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7262690/ https://ncbi.nlm.nih.gov/pubmed/32518793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v8.i10.2001 |
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