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New Screening Tool for Aortic Root Dilation in Children with Marfan Syndrome and Marfan-Like Disorders
One of the roles of a pediatric cardiologist who suspects or diagnoses a genetically determined connective tissue disease (e.g., Marfan, Ehlers–Danlos, and Loeys–Dietz syndromes) is to assess whether the aortic root is dilated. The aortic root diameter is affected by the patient’s age, sex, and body...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer US
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170831/ https://www.ncbi.nlm.nih.gov/pubmed/32006082 http://dx.doi.org/10.1007/s00246-020-02307-0 |