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Five-year response to growth hormone in children with Noonan syndrome and growth hormone deficiency
BACKGROUND: Noonan syndrome (NS) is an autosomal dominant disorder characterized by specific features including short stature, distinctive facial dysmorphic features, congenital heart defects, hypertrophic cardiomyopathy, skeletal anomalies and webbing of the neck. Molecular screening has shown that...
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| Publicado no: | Ital J Pediatr |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4595189/ https://ncbi.nlm.nih.gov/pubmed/26444854 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-015-0183-x |
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