Inside the Noonan “universe”: Literature review on growth, GH/IGF axis and rhGH treatment: Facts and concerns

Noonan syndrome (NS) is a disorder characterized by a typical facial gestalt, congenital heart defects, variable cognitive deficits, skeletal defects, and short stature. NS is caused by germline pathogenic variants in genes coding proteins with a role in the RAS/mitogen-activated protein kinase sign...

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Detalles Bibliográficos
Autores principales: Stagi, Stefano, Ferrari, Vittorio, Ferrari, Marta, Priolo, Manuela, Tartaglia, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434367/
https://www.ncbi.nlm.nih.gov/pubmed/36060964
http://dx.doi.org/10.3389/fendo.2022.951331

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434367/
https://www.ncbi.nlm.nih.gov/pubmed/36060964
http://dx.doi.org/10.3389/fendo.2022.951331

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