Association between Multimorbidity and Quality of Life in 22q11.2 Deletion Syndrome: Cross-section Analysis Using the National Database of Designated Incurable Diseases of Japan
Author:
Affiliation:
1. Department of Neuropsychiatry, The University of Tokyo Hospital
2. Department of Health Services Research, Graduate School of Medicine, The University of Tokyo
Publisher
The Health Care Science Institute
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/iken/33/3/33_2023.002/_pdf
Reference23 articles.
1. Attout L, Noёl MP, Vossius L et al.(2017)“Evidence of the impact of visuo-spatial processing on magnitude representation in 22q11.2 microdeletion syndrome,” Neuropsychologia.99:296-305. https://doi.org/10.1016/j.neuropsychologia.2017.03.023.
2. Bassett AS, Chow EWC, Husted J et al.(2009)“Premature death in adults with 22q11.2 deletion syndrome,” Journal of Medical Genetics.46(5):324-330. https://doi.org/10.1136/jmg.2008.063800.
3. Campbell IM, Sheppard SE, Crowley TB et al.(2018)“What is new with 22q? An update from the 22q and You Center at the Children’s Hospital of Philadelphia,” American Journal of Medical Genetics. Part A.176(10):2058-2069. https://doi.org/10.1002/ajmg.a.40637.
4. De Smedt B , Swillen A, Verschaffel L et al.(2009)“Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review,” Developmental Disabilities Research Reviews.15(1):4-10. https://doi.org/10.1002/ddrr.44.
5. Fung WLA, Butcher NJ, Costain G et al.(2015)“Practical guidelines for managing adults with 22q11.2 deletion syndrome,” Genetics in Medicine: Official Journal of the American College of Medical Genetics.17(8):599-609. https://doi.org/10.1038/gim.2014.175.
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