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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2022
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| 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 |