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1000 Titel
  • Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14
1000 Autor/in
  1. Ihl, Thomas |
  2. Kadas, Ella M. |
  3. Oberwahrenbrock, Timm |
  4. Endres, Matthias |
  5. Klockgether, Thomas |
  6. Schroeter, Jan |
  7. Brandt, Alexander U. |
  8. Paul, Friedemann |
  9. Minnerop, Martina |
  10. Doss, Sarah |
  11. Schmitz-Hübsch, Tanja |
  12. Zimmermann, Hanna G. |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-04-27
1000 Erschienen in
1000 Quellenangabe
  • 19(4):469-482
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s12311-020-01130-w |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351844/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Spinocerebellar ataxia type 14 (SCA-PRKCG, formerly SCA14) is a rare, slowly progressive disorder caused by conventional mutations in protein kinase Cγ (PKCγ). The disease usually manifests with ataxia, but previous reports suggested PRKCG variants in retinal pathology. To systematically investigate for the first time visual function and retinal morphology in patients with SCA-PRKCG. Seventeen patients with PRKCG variants and 17 healthy controls were prospectively recruited, of which 12 genetically confirmed SCA-PRKCG patients and 14 matched controls were analyzed. We enquired a structured history for visual symptoms. Vision-related quality of life was obtained with the National Eye Institute Visual Function Questionnaire (NEI-VFQ) including the Neuro-Ophthalmic Supplement (NOS). Participants underwent testing of visual acuity, contrast sensitivity, visual fields, and retinal morphology with optical coherence tomography (OCT). Measurements of the SCA-PRKCG group were analyzed for their association with clinical parameters (ataxia rating and disease duration). SCA-PRKCG patients rate their vision-related quality of life in NEI-VFQ significantly worse than controls. Furthermore, binocular visual acuity and contrast sensitivity were worse in SCA-PRKCG patients compared with controls. Despite this, none of the OCT measurements differed between groups. NEI-VFQ and NOS composite scores were related to ataxia severity. Additionally, we describe one patient with a genetic variant of uncertain significance in the catalytic domain of PKCγ who, unlike all confirmed SCA-PRKCG, presented with a clinically silent epitheliopathy. SCA-PRKCG patients had reduced binocular vision and vision-related quality of life. Since no structural retinal damage was found, the pathomechanism of these findings remains unclear.
1000 Sacherschließung
lokal Female [MeSH]
lokal Aged [MeSH]
lokal Spinocerebellar Ataxias/complications [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Spinocerebellar ataxias
lokal Middle Aged [MeSH]
lokal Tomography, Optical Coherence [MeSH]
lokal Protein kinase C gamma
lokal Original Article
lokal Vision disorders
lokal Optical coherence tomography
lokal Visual Acuity [MeSH]
lokal Male [MeSH]
lokal Quality of Life [MeSH]
lokal Vision Disorders/genetics [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/SWhsLCBUaG9tYXM=|https://frl.publisso.de/adhoc/uri/S2FkYXMsIEVsbGEgTS4=|https://frl.publisso.de/adhoc/uri/T2JlcndhaHJlbmJyb2NrLCBUaW1t|https://frl.publisso.de/adhoc/uri/RW5kcmVzLCBNYXR0aGlhcw==|https://frl.publisso.de/adhoc/uri/S2xvY2tnZXRoZXIsIFRob21hcw==|https://frl.publisso.de/adhoc/uri/U2Nocm9ldGVyLCBKYW4=|https://frl.publisso.de/adhoc/uri/QnJhbmR0LCBBbGV4YW5kZXIgVS4=|https://frl.publisso.de/adhoc/uri/UGF1bCwgRnJpZWRlbWFubg==|https://frl.publisso.de/adhoc/uri/TWlubmVyb3AsIE1hcnRpbmE=|https://frl.publisso.de/adhoc/uri/RG9zcywgU2FyYWg=|https://frl.publisso.de/adhoc/uri/U2NobWl0ei1Iw7xic2NoLCBUYW5qYQ==|https://frl.publisso.de/adhoc/uri/WmltbWVybWFubiwgSGFubmEgRy4=
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1000 Erstellt am 2023-11-18T15:26:32.248+0100
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