Porphyria cutanea tarda: a case report
Abstract 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...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
BMC
2019-01-01
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Series: | Journal of Medical Case Reports |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13256-018-1956-9 |