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Erythrodontia in congenital erythropoietic porphyria
Congenital erythropoietic porphyria (CEP) is one of the rarest of porphyrias occurring worldwide. CEP is a very rare genetic autosomal recessive disease, with mutation in the gene that codifies uroporphyrinogen-III synthase, leading to porphyrin accumulation in many tissues, with marked skin photose...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications
2011
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3125661/ https://ncbi.nlm.nih.gov/pubmed/21731282 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0973-029X.80022 |
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