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A Case of Congenital Erythropoietic Porphyria without Hemolysis

Porphyrias are group of disorders caused by deficiency of the enzymes in heme synthetic pathway. Congenital erythropoietic porphyria (CEP) is an extremely rare disease with mutation in the gene that codes for uroporphyrinogen III synthase leading to accumulation of porphyrin in different tissues and...

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Detalles Bibliográficos
Autores principales: De, Arun K, Das, Kallol, Sil, Archan, Joardar, Swarnali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778801/
https://www.ncbi.nlm.nih.gov/pubmed/24082206
http://dx.doi.org/10.4103/0019-5154.117336

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