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Assessment of Sleep and Breathing in Adults with Prader-Willi Syndrome: A Case Control Series

OBJECTIVES: Prader-Willi syndrome (PWS) is a genetic disorder (linked to chromosome 15q11-13) characterized by hypotonia and developmental delay, hyperphagia and obesity, hypersomnia and abnormal sleep, and behavioral problems. Such patients may also be at increased risk of obstructive sleep apnea (...

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Detalhes bibliográficos
Main Authors: Yee, Brendon J., Buchanan, Peter R., Mahadev, Sri, Banerjee, Dev, Liu, Peter Y., Phillips, Craig, Loughnan, Georgina, Steinbeck, Kate, Grunstein, Ronald R.
Formato: Artigo
Idioma:Inglês
Publicado em: American Academy of Sleep Medicine 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2556914/
https://ncbi.nlm.nih.gov/pubmed/18198805
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