Study

Sleep Abnormalities in Rare Genetic Disorders: Angelman Syndrome, Rett Syndrome, and Prader-Willi Syndrome

Study ID Alternative Stable ID Type
phs001292 Case-Control

Study Description

This research study will investigate sleep behavior in the rare neurological disorders Angelman Syndrome (AS), Rett Syndrome (RTT), Prader-Willi Syndrome (PWS) and Early-onset Morbid Obesity (EMO). Sleep is very important to proper health and plays a critical role in learning, memory, brain development and brain function. Sleep disturbances can have negative effects on health and the quality of life of children and their families. Sleep disorders are common in individuals with AS, RTT, PWS and EMO. As a result, individuals with AS, RTT, PWS and EMO are at risk for sleep-related health problems that can worsen existing daytime behaviors and lead to additional problems with learning and memory.

The principal objectives of the study are to:

  1. Characterize sleep behavior in individuals with Angelman Syndrome, Rett Syndrome, Prader-Willi Syndrome and Early-onset Morbid Obesity.
  2. Compare sleep behavior in these individuals with sleep behavior in normal controls
  3. Assess the natural history of sleep behavior in individuals with Angelman Syndrome, ... (Show More)

Archive Link Archive Accession
dbGaP phs001292

Who archives the data?

There are no publications available