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Porphyria cutanea tarda: a case report

BACKGROUND: The porphyrias are a rare group of metabolic disorders that can either be inherited or acquired. Along the heme biosynthetic pathway, porphyrias can manifest with neurovisceral and/or cutaneous symptoms, depending on the defective enzyme. Porphyria cutanea tarda, the most common type of...

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Detalles Bibliográficos
Autores principales: Usta Atmaca, Hanife, Akbas, Feray
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340172/
https://www.ncbi.nlm.nih.gov/pubmed/30661508
http://dx.doi.org/10.1186/s13256-018-1956-9

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