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A case of concomitant Gilbert's syndrome and hereditary spherocytosis
We describe moderate hyperbilirubinemia in a 28-year-old man who suffered from gallstones and splenomegaly, with combined disorders of hereditary spherocytosis (HS) and Gilbert's syndrome (GS). Since it is difficult to diagnose HS in the absence of signs of anemia, we evaluated both the genetic...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Korean Association for the Study of the Liver
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3304593/ https://ncbi.nlm.nih.gov/pubmed/20924216 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3350/kjhep.2010.16.3.321 |
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