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...

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Detalles Bibliográficos
Autores principales: Wozniak-Mielczarek, Lidia, Sabiniewicz, Robert, Nowak, Radosław, Gilis-Malinowska, Natasza, Osowicka, Michalina, Mielczarek, Maksymilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Original Article
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

Internet

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

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