Young children with Noonan syndrome: evaluation of feeding problems

Noonan syndrome (NS) is a common genetic syndrome with a high variety in phenotype. Even though genetic testing is possible, NS is still a clinical diagnosis. Feeding problems are often present in infancy. We investigated the feeding status of 108 patients with clinically and genetically confirmed N...

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Detalles Bibliográficos
Autores principales: Draaisma, Jos M. T., Drossaers, Joris, van den Engel-Hoek, Lenie, Leenders, Erika, Geelen, Joyce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547990/
https://www.ncbi.nlm.nih.gov/pubmed/32394265
http://dx.doi.org/10.1007/s00431-020-03664-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547990/
https://www.ncbi.nlm.nih.gov/pubmed/32394265
http://dx.doi.org/10.1007/s00431-020-03664-x

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