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Generalized hyperpigmentation in Wilson's disease: An unusual association
Wilson's disease, an autosomal recessive disorder of copper metabolism, most commonly presents either with hepatic or neurological features. But, it may sometimes have certain atypical presentations posing diagnostic difficulties. We report here a case of Wilson's disease presenting with g...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications & Media Pvt Ltd
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3579056/ https://ncbi.nlm.nih.gov/pubmed/23546359 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-3147.105621 |
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