Sleep Disorders in Childhood Neurogenetic Disorders

被引:5
|
作者
Dosier, Laura Beth Mann [1 ]
Vaughn, Bradley V. [1 ]
Fan, Zheng [1 ]
机构
[1] Univ N Carolina, Dept Neurol, Chapel Hill, NC 27599 USA
来源
CHILDREN-BASEL | 2017年 / 4卷 / 09期
关键词
Neurogenetic; Sleep; Neurodevelopmental; Angelman; Down syndrome; Trisomy; 21; Smith-Magenis; Muchopolysaccharidosis; Achondroplasia; Duchenne; Congenital Central Hypoventilation; PRADER-WILLI-SYNDROME; DUCHENNE MUSCULAR-DYSTROPHY; CONGENITAL CENTRAL HYPOVENTILATION; SMITH-MAGENIS-SYNDROME; EXCESSIVE DAYTIME SLEEPINESS; FORAMEN MAGNUM STENOSIS; ANGELMAN-SYNDROME; DOWN-SYNDROME; BREATHING DISORDERS; UPPER AIRWAY;
D O I
10.3390/children4090082
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Genetic advances in the past three decades have transformed our understanding and treatment of many human diseases including neurogenetic disorders. Most neurogenetic disorders can be classified as rare disease, but collectively neurogenetic disorders are not rare and are commonly encountered in general pediatric practice. The authors decided to select eight relatively well-known neurogenetic disorders including Down syndrome, Angelman syndrome, Prader-Willi syndrome, Smith-Magenis syndrome, congenital central hypoventilation syndrome, achondroplasia, mucopolysaccharidoses, and Duchenne muscular dystrophy. Each disorder is presented in the following format: overview, clinical characteristics, developmental aspects, associated sleep disorders, management and research/future directions.
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页数:29
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