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A timeline of symptom onset and disease progression in CLN3 disease.

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Title: A timeline of symptom onset and disease progression in CLN3 disease.
Authors: Whiteman IT; Batten Disease Support & Research Association Australia, 74 McLachlan Ave, Shelly Beach, NSW, 2261, Australia. research@bdsraaustralia.org.; Batten Disease Support, Research & Advocacy Foundation, Columbus, OH, USA. research@bdsraaustralia.org.; Beyond Batten Disease Foundation, Austin, TX, USA. research@bdsraaustralia.org., Cook AL; Wicking Dementia Research and Education Centre, University of Tasmania, Tasmania, Australia., Augustine EF; Kennedy Krieger Institute, Baltimore, MD, USA., Bindoff AD; Wicking Dementia Research and Education Centre, University of Tasmania, Tasmania, Australia., Johnson AM; Department of Neurology, Sydney Children's Hospital, University of New South Wales, Randwick, NSW, Australia., Mason HL; Coufetery Comms, Medical Writing Services, Mirepoix, France., Mink JW; Consultant, Pittsford, NY, USA., Østergaard JR; Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark., Schulz A; Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Hamburg, Hamburg, Germany., Vermilion J; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA., Vierhile A; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA., Adams HR; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2026 Jan 07; Vol. 21 (1), pp. 38. Date of Electronic Publication: 2026 Jan 07.
Publication Type: Journal Article; Review
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: A timeline of symptom onset and disease progression in CLN3 disease.
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  Data: <searchLink fieldCode="AU" term="%22Whiteman+IT%22">Whiteman IT</searchLink>; Batten Disease Support & Research Association Australia, 74 McLachlan Ave, Shelly Beach, NSW, 2261, Australia. research@bdsraaustralia.org.; Batten Disease Support, Research & Advocacy Foundation, Columbus, OH, USA. research@bdsraaustralia.org.; Beyond Batten Disease Foundation, Austin, TX, USA. research@bdsraaustralia.org.<br /><searchLink fieldCode="AU" term="%22Cook+AL%22">Cook AL</searchLink>; Wicking Dementia Research and Education Centre, University of Tasmania, Tasmania, Australia.<br /><searchLink fieldCode="AU" term="%22Augustine+EF%22">Augustine EF</searchLink>; Kennedy Krieger Institute, Baltimore, MD, USA.<br /><searchLink fieldCode="AU" term="%22Bindoff+AD%22">Bindoff AD</searchLink>; Wicking Dementia Research and Education Centre, University of Tasmania, Tasmania, Australia.<br /><searchLink fieldCode="AU" term="%22Johnson+AM%22">Johnson AM</searchLink>; Department of Neurology, Sydney Children's Hospital, University of New South Wales, Randwick, NSW, Australia.<br /><searchLink fieldCode="AU" term="%22Mason+HL%22">Mason HL</searchLink>; Coufetery Comms, Medical Writing Services, Mirepoix, France.<br /><searchLink fieldCode="AU" term="%22Mink+JW%22">Mink JW</searchLink>; Consultant, Pittsford, NY, USA.<br /><searchLink fieldCode="AU" term="%22Østergaard+JR%22">Østergaard JR</searchLink>; Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark.<br /><searchLink fieldCode="AU" term="%22Schulz+A%22">Schulz A</searchLink>; Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Hamburg, Hamburg, Germany.<br /><searchLink fieldCode="AU" term="%22Vermilion+J%22">Vermilion J</searchLink>; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.<br /><searchLink fieldCode="AU" term="%22Vierhile+A%22">Vierhile A</searchLink>; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.<br /><searchLink fieldCode="AU" term="%22Adams+HR%22">Adams HR</searchLink>; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
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  Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2026 Jan 07; Vol. 21 (1), pp. 38. <i>Date of Electronic Publication: </i>2026 Jan 07.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41501856
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        Value: 10.1186/s13023-025-04174-5
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              Text: 2026 Jan 07
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