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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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Bibliografski detalji
Glavni autori: Bhavasar, Rashmi, Santoshkumar, G, Prakash, B Rahul
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications 2011
Teme:
Online pristup: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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