Growth, Endocrine Features, and Growth Hormone Treatment in Noonan Syndrome

Noonan syndrome is a heterogeneous congenital disorder. The main features are typical facial features, short stature and cardiac defects. The diagnosis is clinical: in 80% of patients with Noonan syndrome a genetic defect can be shown. Inheritance is predominantly autosomal dominant and seldom autos...

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Detalles Bibliográficos
Autores principales: Dahlgren, Jovanna, Noordam, Cees
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999676/
https://www.ncbi.nlm.nih.gov/pubmed/35407641
http://dx.doi.org/10.3390/jcm11072034

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999676/
https://www.ncbi.nlm.nih.gov/pubmed/35407641
http://dx.doi.org/10.3390/jcm11072034

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