| Literature DB >> 20699055 |
Kathryn E Thomas1, Daniel Fletcher, Mina Mottahedeh.
Abstract
Acute intermittent porphyria (AIP) is a rare, inherited metabolic disorder of the haem biosynthesis pathway. The diagnosis is well known to cause significant diagnostic challenge due to its broad range of symptoms that may mimic many other conditions. We report a case of AIP that presented with caecal perforation, a clinical scenario that has not previously been reported in the literature.Entities:
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Year: 2010 PMID: 20699055 PMCID: PMC5697001 DOI: 10.1308/147870810X12699662981834
Source DB: PubMed Journal: Ann R Coll Surg Engl ISSN: 0035-8843 Impact factor: 1.891