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Case report of Barth syndrome: a forgotten cause of cardiomyopathy
BACKGROUND: Barth syndrome (BTHS) is a rare X-linked recessive disorder characterized by clinical features including cardiomyopathy, skeletal myopathy, neutropenia, growth delay, and exercise intolerance. It is often considered to be a paediatric disease, owing to most cases being diagnosed during c...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453413/ https://www.ncbi.nlm.nih.gov/pubmed/34557625 http://dx.doi.org/10.1093/ehjcr/ytab195 |