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Drug treatment in acute porphyria
The acute hepatic porphyrias are rare pharmacogenetic diseases inherited as autosomal dominant conditions of low penetrance. The genetic defect is a 50% deficiency of an enzyme of the haem biosynthetic pathway. Patients may develop ‘neurovisceral attacks’ which include severe abdominal pain, neurops...
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
1997
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| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2042871/ https://ncbi.nlm.nih.gov/pubmed/9384458 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2125.1997.t01-1-00609.x |
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