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Congenital erythropoietic porphyria (Gunther disease): a case report
Congenital erythropoietic porphyria (CEP or Gunther disease) is a very rare subtype of porphyria with a prevalence of <0.9 per 1 000 000. A 13-year-old female patient came to our hospital complaining of a severe cutaneous ulceration and scarring. The symptoms began in her first year of life as ur...
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| Publicado en: | Oxf Med Case Reports |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7376977/ https://ncbi.nlm.nih.gov/pubmed/32728454 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omaa051 |
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