Hypogonadism in Patients with Prader Willi Syndrome: A Narrative Review

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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Bibliographic Details
Main Authors: Luigi Napolitano, Biagio Barone, Simone Morra, Giuseppe Celentano, Roberto La Rocca, Marco Capece, Vincenzo Morgera, Carmine Turco, Vincenzo Francesco Caputo, Gianluca Spena, Lorenzo Romano, Luigi De Luca, Gianluigi Califano, Claudia Collà Ruvolo, Francesco Mangiapia, Vincenzo Mirone, Nicola Longo, Massimiliano Creta
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:International Journal of Molecular Sciences
Subjects:
Prader-Willi syndrome
hypogonadism
chromosome 15 abnormalities
genomic imprinting
Online Access:https://www.mdpi.com/1422-0067/22/4/1993

Internet

https://www.mdpi.com/1422-0067/22/4/1993

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