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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Detalles Bibliográficos
Autores principales: Bhavasar, Rashmi, Santoshkumar, G, Prakash, B Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125661/
https://www.ncbi.nlm.nih.gov/pubmed/21731282
http://dx.doi.org/10.4103/0973-029X.80022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125661/
https://www.ncbi.nlm.nih.gov/pubmed/21731282
http://dx.doi.org/10.4103/0973-029X.80022

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