Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults-Reference-Cited by-同舟云学术

Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults

Published:2022-08-25 Issue:12 Volume:30 Page:1314-1317
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Boot Erik^ORCID,Marras Connie,Bassett Anne S.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://www.nature.com/articles/s41431-022-01152-4.pdf

Reference10 articles.

1. McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, et al. 22q11.2 deletion syndrome. Nat Rev Dis Prim. 2015;1:15071.

2. Boot E, Mentzel TQ, Palmer LD, van Harten PN, Marras C, Lang AE, et al. Age-related parkinsonian signs in microdeletion 22q11.2. Mov Disord. 2020;35:1239–45.

3. Boot E, Bassett AS, Marras C. 22q11.2 deletion syndrome-associated Parkinson’s disease. Mov Disord Clin Pract. 2019;6:11–6.

4. McNeill A. Movement disorders in adults with 22q11 deletion syndrome. Mov Disord Clin Pr. 2019;6:339.

5. Cheung EN, George SR, Costain GA, Andrade DM, Chow EW, Silversides CK, et al. Prevalence of hypocalcaemia and its associated features in 22q11.2 deletion syndrome. Clin Endocrinol. 2014;81:190–6.

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