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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zavras, Niki, Meazza, Cristina, Pilotta, Alba, Gertosio, Chiara, Pagani, Sara, Tinelli, Carmine, Bozzola, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595189/
https://www.ncbi.nlm.nih.gov/pubmed/26444854
http://dx.doi.org/10.1186/s13052-015-0183-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595189/
https://www.ncbi.nlm.nih.gov/pubmed/26444854
http://dx.doi.org/10.1186/s13052-015-0183-x

Ejemplares similares