Sleep Disorders in Childhood Neurogenetic Disorders

dc.contributor.author

Dosier, Laura

dc.contributor.author

Vaughn, Bradley

dc.contributor.author

Fan, Zheng

dc.date.accessioned

2019-07-12T20:28:17Z

dc.date.available

2019-07-12T20:28:17Z

dc.date.issued

2017-09-12

dc.date.updated

2019-07-12T20:28:16Z

dc.description.abstract

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.

dc.identifier.issn

2227-9067

dc.identifier.issn

2227-9067

dc.identifier.uri

https://hdl.handle.net/10161/19099

dc.language

English

dc.publisher

MDPI AG

dc.relation.ispartof

Children

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10.3390/children4090082

dc.subject

Neurogenetic

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Sleep

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Neurodevelopmental

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Angelman

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Down Syndrome

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Trisomy 21

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Smith-Magenis

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Muchopolysaccharidoses

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Achondroplasia

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Duchenne

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Congenital Central hypoventilation

dc.title

Sleep Disorders in Childhood Neurogenetic Disorders

dc.type

Journal article

pubs.issue

9

pubs.organisational-group

School of Medicine

pubs.organisational-group

Duke

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Pediatrics, Pulmonary and Sleep Medicine

pubs.organisational-group

Pediatrics

pubs.organisational-group

Clinical Science Departments

pubs.publication-status

Accepted

pubs.volume

4

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