Dilated coronary arteries in a 2-month-old with RIT1-associated Noonan syndrome: a case report

BACKGROUND: Noonan Syndrome is caused by variants in a variety of genes found in the RAS/MAPK pathway. As more causative genes for Noonan Syndrome have been identified, more phenotype variability has been found, particularly congenital heart defects. Here, we report a case of dilated coronary arteri...

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Detalles Bibliográficos
Autores principales: Aniol, Claudia V., Prokop, Jeremy W., Rajasekaran, Surender, Pageau, Spencer, Elizer, Sydney K., VanSickle, Elizabeth A., Bupp, Caleb P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806447/
https://www.ncbi.nlm.nih.gov/pubmed/36593444
http://dx.doi.org/10.1186/s12887-022-03818-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806447/
https://www.ncbi.nlm.nih.gov/pubmed/36593444
http://dx.doi.org/10.1186/s12887-022-03818-w

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