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Differences in severity of cardiovascular anomalies in children with Noonan syndrome based on the causative gene
BACKGROUND: Noonan syndrome (NS) is a genetic syndrome, characterized by various dysmorphic features, cardiac anomalies, short stature, and developmental delay. NS is a leading cause of cardiovascular anomalies. The syndrome results from dysregulation in the RAS-MAPK pathway and is related to the RA...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9492920/ https://www.ncbi.nlm.nih.gov/pubmed/36160796 http://dx.doi.org/10.3389/fped.2022.946071 |