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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158928/ https://www.ncbi.nlm.nih.gov/pubmed/30302293 http://dx.doi.org/10.1155/2018/3232105 |