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The acute hepatic porphyrias
The acute hepatic porphyrias (AHP) are a group of four inherited diseases of heme biosynthesis. They present with similar severe, episodic, acute neurovisceral symptoms due to abnormally elevated levels of porphyrin precursors delta-aminolevulinic acid (ALA). Recently genetic screening indicates tha...
保存先:
| 出版年: | Transl Gastroenterol Hepatol |
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| 第一著者: | |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
AME Publishing Company
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7838531/ https://ncbi.nlm.nih.gov/pubmed/33824928 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/tgh-2020-01 |
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