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  2. Obstructive sleep apnea - Wikipedia

    en.wikipedia.org/wiki/Obstructive_sleep_apnea

    A little over 50% of all people with Down syndrome experience obstructive sleep apnea, [59] and some physicians advocate routine testing of this group. [60] In other craniofacial syndromes, the abnormal feature may actually improve the airway, but its correction may put the person at risk for obstructive sleep apnea after surgery when it is ...

  3. Sleep apnea: causes, symptoms, treatments, and how it ... - AOL

    www.aol.com/lifestyle/sleep-apnea-causes...

    Obstructive sleep apnea can be categorized as mild, moderate or severe. Mild sleep apnea: 5-15 apnea or hypopnea events per hour Moderate sleep apnea: 15-30 events per hour

  4. Sleep apnea - Wikipedia

    en.wikipedia.org/wiki/Sleep_apnea

    More than half of people with obstructive sleep apnea have some degree of positional obstructive sleep apnea, meaning that it gets worse when they sleep on their backs. [69] Sleeping on their sides is an effective and cost-effective treatment for positional obstructive sleep apnea. [69]

  5. What Is Sleep Apnea? Your Complete Guide - AOL

    www.aol.com/sleep-apnea-complete-guide-115800238...

    Sleep apnea is a common sleep disorder that affects more than 20 percent of people in the United States. ... Obstructive sleep apnea (OSA). ... The device sends mild electrical impulses to the ...

  6. Sleep-related breathing disorder - Wikipedia

    en.wikipedia.org/wiki/Sleep-related_breathing...

    Sleep apnea is measured by the apnea-hypopnea index (AHI). An AHI is determined with a sleep study. AHI values for adults are categorized as: [2] [3] Normal: AHI<5; Mild sleep apnea: 5≤AHI<15; Moderate sleep apnea: 15≤AHI<30; Severe sleep apnea: AHI≥30; An episode is when a person hesitates to breathe or stops their breathing altogether.

  7. Xia–Gibbs syndrome - Wikipedia

    en.wikipedia.org/wiki/Xia–Gibbs_syndrome

    In 2014, a human genetic disorder (Xia-Gibbs syndrome) caused by de novo mutations in AHDC1 was discovered through whole-exome sequencing by Xia, et al. [6] Four patients were identified in the paper which recorded the initial discovery and their clinical features were reported, including global developmental delay, hypotonia, obstructive sleep apnea, intellectual disability and seizures.

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