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Microsaccadic pursuit

MedGen UID:
334855
Concept ID:
C1843892
Finding
HPO: HP:0007792

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVMicrosaccadic pursuit

Conditions with this feature

Spinocerebellar ataxia type 21
MedGen UID:
375311
Concept ID:
C1843891
Disease or Syndrome
Spinocerebellar ataxia-21 (SCA21) is an autosomal dominant neurologic disorder characterized by onset in the first decades of life of slowly progressive cerebellar ataxia, which is associated with cognitive impairment in most patients (summary by Delplanque et al., 2014). For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400).

Recent clinical studies

Therapy

Badler JB, Watamaniuk SNJ, Heinen SJ
J Neurophysiol 2019 Nov 1;122(5):1981-1988. Epub 2019 Sep 18 doi: 10.1152/jn.00198.2019. PMID: 31533016
Hafed ZM, Clark JJ
Vision Res 2002 Oct;42(22):2533-45. doi: 10.1016/s0042-6989(02)00263-8. PMID: 12445847

Prognosis

Ziv I, Bonneh YS
J Vis 2021 Feb 3;21(2):12. doi: 10.1167/jov.21.2.12. PMID: 33630026Free PMC Article
Badler JB, Watamaniuk SNJ, Heinen SJ
J Neurophysiol 2019 Nov 1;122(5):1981-1988. Epub 2019 Sep 18 doi: 10.1152/jn.00198.2019. PMID: 31533016
Kornilova L, Grigorova V, Mueller Ch, Sagalovitch SV, Alekhina M, Kozlovskaya I
J Gravit Physiol 2004 Jul;11(2):P5-7. PMID: 16229108

Clinical prediction guides

Watamaniuk SNJ, Badler JB, Heinen SJ
Sci Rep 2023 May 7;13(1):7418. doi: 10.1038/s41598-023-34066-2. PMID: 37150766Free PMC Article
Ziv I, Bonneh YS
J Vis 2021 Feb 3;21(2):12. doi: 10.1167/jov.21.2.12. PMID: 33630026Free PMC Article
Badler JB, Watamaniuk SNJ, Heinen SJ
J Neurophysiol 2019 Nov 1;122(5):1981-1988. Epub 2019 Sep 18 doi: 10.1152/jn.00198.2019. PMID: 31533016
Gibaldi A, Vanegas M, Bex PJ, Maiello G
Behav Res Methods 2017 Jun;49(3):923-946. doi: 10.3758/s13428-016-0762-9. PMID: 27401169Free PMC Article

Supplemental Content

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