Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 May 27;7(6):57.
doi: 10.3390/brainsci7060057.

Acute Regression in Young People with Down Syndrome

Affiliations

Acute Regression in Young People with Down Syndrome

Clotilde Mircher et al. Brain Sci. .

Abstract

Abstract: Adolescents and young adults with Down syndrome (DS) can present a rapid regression with loss of independence and daily skills. Causes of regression are unknown and treatment is most of the time symptomatic. We did a retrospective cohort study of regression cases: patients were born between 1959 and 2000, and were followed from 1984 to now. We found 30 DS patients aged 11 to 30 years old with history of regression. Regression occurred regardless of the cognitive level (severe, moderate, or mild intellectual disability (ID)). Patients presented psychiatric symptoms (catatonia, depression, delusions, stereotypies, etc.), partial or total loss of independence in activities of daily living (dressing, toilet, meals, and continence), language impairment (silence, whispered voice, etc.), and loss of academic skills. All patients experienced severe emotional stress prior to regression, which may be considered the trigger. Partial or total recovery was observed for about 50% of them. In our cohort, girls were more frequently affected than boys (64%). Neurobiological hypotheses are discussed as well as preventative and therapeutic approaches.

Keywords: adolescence; down syndrome; neurobiology; regression.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

References

    1. Stoll C., Alembik Y., Dott B., Roth M.P. Recent trends in the prevalence of Down syndrome in north-eastern France. Ann. Genet. 1994;37:179–183. - PubMed
    1. Jacobs J., Schwartz A., McDougle C.J., Skotko B.G. Rapid clinical deterioration in an individual with Down syndrome. Am. J. Med. Genet. A. 2016;170:1899–1902. doi: 10.1002/ajmg.a.37674. - DOI - PubMed
    1. Worley G., Crissman B.G., Cadogan E., Milleson C., Adkins D.W. Down syndrome disintegrative disorder: New-onset autistic regression, dementia, and insomnia in older children and adolescents with Down syndrome. J. Child Neurol. 2015;30:1147–1152. doi: 10.1177/0883073814554654. - DOI - PubMed
    1. Ghaziuddin N., Nassiri A., Miles J.H. Catatonia in Down syndrome; a treatable cause of regression. Neuropsychiatr. Dis. Treat. 2015;11:941–949. doi: 10.2147/NDT.S77307. - DOI - PMC - PubMed
    1. Stoll C., Dott B., Alembik Y., Roth M.-P. Associated congenital anomalies among cases with Down syndrome. Eur. J. Med. Genet. 2015;58:674–680. doi: 10.1016/j.ejmg.2015.11.003. - DOI - PubMed

LinkOut - more resources