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Black Aortic Valve: Incidental Finding of Alkaptonuria
Background Alkaptonuria is a rare autosomal recessive genetic disorder of tyrosine metabolism, which results in accumulation of homogentisic acid in various tissues, including the cardiovascular system. Case Description We report on a 64-year-old man with mixed aortic valve disease who underwent c...
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| Vydáno v: | Thorac Cardiovasc Surg Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Georg Thieme Verlag KG
2021
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8236329/ https://ncbi.nlm.nih.gov/pubmed/34194920 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0041-1728721 |
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