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Unexplained regression in Down syndrome: 35 cases from an international Down syndrome database.

Publication ,  Journal Article
Santoro, SL; Cannon, S; Capone, G; Franklin, C; Hart, SJ; Hobensack, V; Kishnani, PS; Macklin, EA; Manickam, K; McCormick, A; Nash, P ...
Published in: Genet Med
April 2020

PURPOSE: An entity of regression in Down syndrome (DS) exists that affects adolescents and young adults and differs from autism spectrum disorder and Alzheimer disease. METHODS: Since 2017, an international consortium of DS clinics assembled a database of patients with unexplained regression and age- and sex-matched controls. Standardized data on clinical symptoms and tiered medical evaluations were collected. Elements of the proposed definition of unexplained regression in DS were analyzed by paired comparisons between regression cases and matched controls. RESULTS: We identified 35 patients with DS and unexplained regression, with a mean age at regression of 17.5 years. Diagnostic features differed substantially between regression cases and matched controls (p < 0.001 for all but externalizing behaviors). Patients with regression had four times as many mental health concerns (p < 0.001), six times as many stressors (p < 0.001), and seven times as many depressive symptoms (p < 0.001). Tiered medical evaluation most often identified abnormalities in vitamin D 25-OH levels, polysomnograms, thyroid peroxidase antibodies, and celiac screens. Analysis of the subset of patients with nondiagnostic medical evaluations reinforced the proposed definition. CONCLUSIONS: Our case-control evidence supports a proposed definition of unexplained regression in Down syndrome. Establishing this clinical definition supports future research and investigation of an underlying mechanism.

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Published In

Genet Med

DOI

EISSN

1530-0366

Publication Date

April 2020

Volume

22

Issue

4

Start / End Page

767 / 776

Location

United States

Related Subject Headings

  • Young Adult
  • Humans
  • Genetics & Heredity
  • Down Syndrome
  • Databases, Factual
  • Case-Control Studies
  • Autism Spectrum Disorder
  • Adolescent
  • 3105 Genetics
  • 1103 Clinical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
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Santoro, S. L., Cannon, S., Capone, G., Franklin, C., Hart, S. J., Hobensack, V., … Skotko, B. G. (2020). Unexplained regression in Down syndrome: 35 cases from an international Down syndrome database. Genet Med, 22(4), 767–776. https://doi.org/10.1038/s41436-019-0706-8
Santoro, Stephanie L., Sheila Cannon, George Capone, Cathy Franklin, Sarah J. Hart, Victoria Hobensack, Priya S. Kishnani, et al. “Unexplained regression in Down syndrome: 35 cases from an international Down syndrome database.Genet Med 22, no. 4 (April 2020): 767–76. https://doi.org/10.1038/s41436-019-0706-8.
Santoro SL, Cannon S, Capone G, Franklin C, Hart SJ, Hobensack V, et al. Unexplained regression in Down syndrome: 35 cases from an international Down syndrome database. Genet Med. 2020 Apr;22(4):767–76.
Santoro, Stephanie L., et al. “Unexplained regression in Down syndrome: 35 cases from an international Down syndrome database.Genet Med, vol. 22, no. 4, Apr. 2020, pp. 767–76. Pubmed, doi:10.1038/s41436-019-0706-8.
Santoro SL, Cannon S, Capone G, Franklin C, Hart SJ, Hobensack V, Kishnani PS, Macklin EA, Manickam K, McCormick A, Nash P, Oreskovic NM, Patsiogiannis V, Steingass K, Torres A, Valentini D, Vellody K, Skotko BG. Unexplained regression in Down syndrome: 35 cases from an international Down syndrome database. Genet Med. 2020 Apr;22(4):767–776.

Published In

Genet Med

DOI

EISSN

1530-0366

Publication Date

April 2020

Volume

22

Issue

4

Start / End Page

767 / 776

Location

United States

Related Subject Headings

  • Young Adult
  • Humans
  • Genetics & Heredity
  • Down Syndrome
  • Databases, Factual
  • Case-Control Studies
  • Autism Spectrum Disorder
  • Adolescent
  • 3105 Genetics
  • 1103 Clinical Sciences