Hypogonadism in Patients with Prader Willi Syndrome: A Narrative Review

Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder related to the lack of a functional paternal copy of chromosome 15q11-q13. Several clinical manifestations are reported, such as short stature, cognitive and behavioral disability, temperature instability, hypotonia, hypersomnia...

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Detalles Bibliográficos
Autores principales: Napolitano, Luigi, Barone, Biagio, Morra, Simone, Celentano, Giuseppe, La Rocca, Roberto, Capece, Marco, Morgera, Vincenzo, Turco, Carmine, Caputo, Vincenzo Francesco, Spena, Gianluca, Romano, Lorenzo, De Luca, Luigi, Califano, Gianluigi, Collà Ruvolo, Claudia, Mangiapia, Francesco, Mirone, Vincenzo, Longo, Nicola, Creta, Massimiliano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922674/
https://www.ncbi.nlm.nih.gov/pubmed/33671467
http://dx.doi.org/10.3390/ijms22041993

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922674/
https://www.ncbi.nlm.nih.gov/pubmed/33671467
http://dx.doi.org/10.3390/ijms22041993

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