% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Wagemann:163951,
      author       = {Wagemann, Olivia and Loosli, Sandra V and Vöglein,
                      Jonathan and Prix, Catharina and Wlasich, Elisabeth and
                      Nuebling, Georg Sebastian Otto and Danek, Adrian and Levin,
                      Johannes},
      title        = {{R}egression bei jungen {E}rwachsenen mit einem
                      {D}own-{S}yndrom: {E}ine {F}allserie.},
      journal      = {Fortschritte der Neurologie, Psychiatrie},
      volume       = {90},
      number       = {10},
      issn         = {0015-8194},
      address      = {Stuttgart [u.a.]},
      publisher    = {Thieme},
      reportid     = {DZNE-2022-00625},
      pages        = {465-470},
      year         = {2022},
      abstract     = {Regression in young adults with Down syndrome can present
                      itself with an acute loss of acquired skills and change in
                      behavior. The aim of our case series was to describe the
                      heterogeneous clinical presentation of this syndrome as well
                      as accompanying diagnostic and therapeutic challenges and
                      consequences.All three patients were assessed with the
                      CAMDEX-DS (Cambridge Examination for Mental Disorders of
                      Older People with Down Syndrome and Others with Intellectual
                      Disabilities) and the criteria published by the DSMIG-USA
                      (Down-Syndrome Medical Interest Group USA).After ruling out
                      somatic or other psychiatric causes, the application of the
                      DSMIG-USA criteria resulted in diagnosing at least a
                      probable unexplained regression in all three patients.The
                      thorough diagnostic investigation of unexplained acute
                      regression in young adults with Down syndrome allows for
                      quick initiation of therapeutic and supportive measures.
                      Using the DMSIG-USA criteria facilitates the assessment of
                      the underlying diffuse and heterogenous pathology.},
      keywords     = {Aged / Cognition / Down Syndrome: complications / Humans /
                      Intellectual Disability: complications / Young Adult},
      cin          = {AG Höglinger 1 / AG Höglinger 2 / Clinical Dementia
                      Research München},
      ddc          = {150},
      cid          = {I:(DE-2719)1110002 / I:(DE-2719)1111015 /
                      I:(DE-2719)1111016},
      pnm          = {353 - Clinical and Health Care Research (POF4-353)},
      pid          = {G:(DE-HGF)POF4-353},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:35405744},
      doi          = {10.1055/a-1743-2915},
      url          = {https://pub.dzne.de/record/163951},
}