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Cardiac events in Costello syndrome: One case and a review of the literature
Costello syndrome is a rare syndrome associated with de novo mutations in the HRAS gene. It is mostly revealed during in the first months of life by growth retardation, facial dysmorphic features, skin and cardiac abnormalities and subsequent cognitive deficit of varying severity. We report a case o...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3978860/ https://ncbi.nlm.nih.gov/pubmed/24719541 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jsha.2013.11.002 |
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