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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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Bibliografski detalji
Glavni autori: Hakim, Kaouthar, Boussaada, Rafik, Hamdi, Imen, Msaad, Hela
Format: Artigo
Jezik:Inglês
Izdano: 2013
Teme:
Online pristup: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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