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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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| I publikationen: | Eur J Pediatr |
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| Huvudupphovsmän: | , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Springer Berlin Heidelberg
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7547990/ https://ncbi.nlm.nih.gov/pubmed/32394265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00431-020-03664-x |
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