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Primary Carnitine Deficiency: A Rare, Reversible Metabolic Cardiomyopathy
A 24-year-old female with a diagnosis of primary carnitine deficiency, a rare inherited metabolic disorder predominantly described in the paediatric literature that causes cardiomyopathy, presented for evaluation after three months of nonadherence with prescribed carnitine therapy. Initial echocardi...
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| Publicado no: | Case Rep Cardiol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6158928/ https://ncbi.nlm.nih.gov/pubmed/30302293 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/3232105 |
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