Polysomnographic findings in children with 22q deletion & duplication syndrome: relationship to genetic diagnosis, parent-reported symptoms, and calcium levels-Reference-Cited by-同舟云学术

Polysomnographic findings in children with 22q deletion & duplication syndrome: relationship to genetic diagnosis, parent-reported symptoms, and calcium levels

Published:2023-08-01 Issue: Volume: Page:
ISSN:1520-9512
Container-title:Sleep and Breathing
language:en
Short-container-title:Sleep Breath

Author:

Ingram David G.^ORCID,Tracy Meghan,Noel-MacDonnell Janelle,Ghulmiyyah Jana M.,Arganbright Jill M.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Otorhinolaryngology

Link

https://link.springer.com/content/pdf/10.1007/s11325-023-02897-y.pdf

Reference19 articles.

1. Bassett AS et al (2011) Practical guidelines for managing patients with 22q11.2 deletion syndrome. J Pediatr 159(2):332–9.e1

2. Arganbright JM et al (2020) Sleep patterns and problems among children with 22q11 deletion syndrome. Mol Genet Genomic Med 8(6):e1153

3. Ingram DG, Raje N, Arganbright JM (2022) Sleep profiles in children with 22q deletion syndrome: a study of 100 consecutive children seen in a multidisciplinary clinic. J Clin Sleep Med 19(1):27–34

4. Leader G et al (2020) Relationship between parent-reported gastrointestinal symptoms, sleep problems, autism spectrum disorder symptoms, and behavior problems in children and adolescents with 22q11.2 deletion syndrome. Res Dev Disabil 104:103698

5. Hyde J et al (2021) Gene deletion and sleep depletion: exploring the relationship between sleep and affect in 22q11.2 deletion syndrome. J Genet Psychol 182(5):304–316

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