Article

"Sleep Respiratory Profiles Across Genetic Subtypes of Prader-Willi Syndrome: An Exploratory Polysomnographic Study"

2026-08-01

Abstract excerpt

Prader-Willi Syndrome (PWS) is a rare genetic disorder defined by three different types of genetic mutation: deletion (PWS DEL ), maternal uniparental disomy (PWS UPD ), and imprinting center defects (PWS IMP ). Sleep-related disorders have been described in children with PWS; however, the role of respiratory measures during sleep in these patients remains unclear, particularly concerning specific genetic mutation...

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Literature Corpus work: 15c22a8a-770b-5c06-810b-886bf696e058
DOI: 10.1016/j.sleepe.2026.100161

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