Liver Transplantation for Acute Intermittent Porphyria is Complicated by a High Rate of Hepatic Artery Thrombosis
Acute intermittent porphyria (AIP) is an autosomal-dominant condition resulting from a partial deficiency of the ubiquitously expressed enzyme porphobilinogen deaminase. Although its clinical expression is highly variable, a minority of patients suffer recurrent life-threatening neurovisceral attack...
Main Authors: | , , , , , |
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Format: | Online |
Language: | English |
Published: |
Wiley Subscription Services, Inc., A Wiley Company
2012
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472026/ |