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Article

Young children with Noonan syndrome: evaluation of feeding problems.

European journal of pediatrics - 1 Nov 2020

Draaisma Jos M T, Drossaers Joris, van den Engel-Hoek Lenie, Leenders Erika, Geelen Joyce

Abstract excerpt

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 NS. Only patients with a documented feeding status before the age of 6 were included. A distinction was made between...

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Identifiers

PMID: 32394265
DOI: 10.1007/s00431-020-03664-x
PMCID: PMC7547990

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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