Skip to main content
SpringerLink
Log in

Rare genetic disorders and the heightened importance of baseline motor examinations in children and adolescents experiencing a first episode of psychosis

  • Correspondence
  • Published:
European Child & Adolescent Psychiatry Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  1. Boot E, Marras C, Bassett AS (2022) Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: comment on the literature and retrospective study of 92 adults. Eur J Hum Genet 30:1314–1317

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Haldeman-Englert CR, Jewett T (1993) 1q21.1 Recurrent Microdeletion. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A (eds) GeneReviews((R)). Seattle (WA)

  3. Marshall CR, Howrigan DP, Merico D, Thiruvahindrapuram B, Wu W, Greer DS, Antaki D, Shetty A, Holmans PA, Pinto D, Gujral M, Brandler WM, Malhotra D, Wang Z, Fajarado KVF, Maile MS, Ripke S, Agartz I, Albus M, Alexander M, Amin F, Atkins J, Bacanu SA, Belliveau RA Jr., Bergen SE, Bertalan M, Bevilacqua E, Bigdeli TB, Black DW, Bruggeman R, Buccola NG, Buckner RL, Bulik-Sullivan B, Byerley W, Cahn W, Cai G, Cairns MJ, Campion D, Cantor RM, Carr VJ, Carrera N, Catts SV, Chambert KD, Cheng W, Cloninger CR, Cohen D, Cormican P, Craddock N, Crespo-Facorro B, Crowley JJ, Curtis D, Davidson M, Davis KL, Degenhardt F, Del Favero J, DeLisi LE, Dikeos D, Dinan T, Djurovic S, Donohoe G, Drapeau E, Duan J, Dudbridge F, Eichhammer P, Eriksson J, Escott-Price V, Essioux L, Fanous AH, Farh KH, Farrell MS, Frank J, Franke L, Freedman R, Freimer NB, Friedman JI, Forstner AJ, Fromer M, Genovese G, Georgieva L, Gershon ES, Giegling I, Giusti-Rodriguez P, Godard S, Goldstein JI, Gratten J, de Haan L, Hamshere ML, Hansen M, Hansen T, Haroutunian V, Hartmann AM, Henskens FA, Herms S, Hirschhorn JN, Hoffmann P, Hofman A, Huang H, Ikeda M, Joa I, Kahler AK et al (2017) Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nat Genet 49:27–35

  4. Martin CL, Ledbetter DH (2017) Chromosomal microarray testing for Children with Unexplained Neurodevelopmental disorders. JAMA 317:2545–2546

    Article  PubMed  PubMed Central  Google Scholar 

  5. Morris CA, Mervis CB, Paciorkowski AP, Abdul-Rahman O, Dugan SL, Rope AF, Bader P, Hendon LG, Velleman SL, Klein-Tasman BP, Osborne LR (2015) 7q11.23 duplication syndrome: physical characteristics and natural history. Am J Med Genet A 167A:2916–2935

    Article  PubMed  PubMed Central  Google Scholar 

  6. Pieters LE, Nadesalingam N, Walther S, van Harten PN (2022) A systematic review of the prognostic value of motor abnormalities on clinical outcome in psychosis. Neurosci Biobehav Rev 132:691–705

    Article  PubMed  Google Scholar 

  7. Trakadis YJ, Fulginiti V, Walterfang M (2018) Inborn errors of metabolism associated with psychosis: literature review and case-control study using exome data from 5090 adult individuals. J Inherit Metab Dis 41:613–621

    Article  CAS  PubMed  Google Scholar 

  8. Ueda K, Shinawi M, Pearson TS (2021) Paroxysmal kinesigenic dyskinesia in Twins with chromosome 16p11.2 duplication syndrome. Neurol Genet 7:e549

    Article  PubMed  PubMed Central  Google Scholar 

  9. van de Burgt N, van Doesum W, Grevink M, van Niele S, de Koning T, Leibold N, Martinez-Martinez P, van Amelsvoort T, Cath D (2023) Psychiatric manifestations of inborn errors of metabolism: a systematic review. Neurosci Biobehav Rev 144:104970

    Article  PubMed  Google Scholar 

  10. van Harten PN, Walther S, Kent JS, Sponheim SR, Mittal VA (2017) The clinical and prognostic value of motor abnormalities in psychosis, and the importance of instrumental assessment. Neurosci Biobehav Rev 80:476–487

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

The author has no relevant financial or non-financial interests to disclose.

Author information

Authors and Affiliations

  1. Department of Psychiatry, Hotchkiss Brain Institute, Mathison Centre for Mental Health Research and Education, The University of Calgary, Calgary, AB, Canada

    Mark Ainsley Colijn

Authors
  1. Mark Ainsley Colijn
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Mark Colijn is the sole author and was responsible for the development and writing of this letter.

Corresponding author

Correspondence to Mark Ainsley Colijn.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The author declares no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Colijn, M.A. Rare genetic disorders and the heightened importance of baseline motor examinations in children and adolescents experiencing a first episode of psychosis. Eur Child Adolesc Psychiatry (2024). https://doi.org/10.1007/s00787-024-02449-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00787-024-02449-z

Search

Navigation