044. Sleep apnoea syndrome after growth hormone therapy in a patient with Prader-Willi syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a rare genetic disorder, which incidence is 1/10,000-1/30,000. It is characterized by hypotonia, short stature, delayed motor and mental development, hypogonadism, hyperphagia, obesity and specific physical appearance. It has been observed increased frequen...

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Salvato in:
Dettagli Bibliografici
Pubblicato in:J Thorac Dis
Autori principali: Nikolaou, Konstantina, Papagianni, Maria, Siopi, Dimitra, Markopoulou, Katerina, Kareklas, Nikos, Galanou, Artemis, Agrafiotis, Michalis, Tsara, Venetia
Natura: Artigo
Lingua:Inglês
Pubblicazione: AME Publishing Company 2015
Soggetti:
The Pan Hellenic Congress Abstracts
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4332108/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2072-1439.2015.AB044
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