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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...
Autores principales: | Usta Atmaca, Hanife, Akbas, Feray |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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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