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Late-onset multiple acyl-CoA dehydrogenase deficiency with cardiac syncope: A case report
BACKGROUND: Multiple acyl-CoA dehydrogenase deficiency (MADD) is an uncommon autosomal recessive disorder of mitochondrial fatty acid beta-oxidation. Syncope is a transient loss of consciousness due to acute global cerebral hypoperfusion. Late-onset MADD with syncope has not been reported previously...
Tallennettuna:
| Julkaisussa: | World J Clin Cases |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Baishideng Publishing Group Inc
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7062611/ https://ncbi.nlm.nih.gov/pubmed/32190638 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v8.i5.995 |
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