Nystagmus characteristics in congenital stationary night blindness (CSNB)

被引:21
|
作者
Pieh, C. [1 ]
Simonsz-Toth, B. [2 ]
Gottlob, I. [3 ]
机构
[1] Univ Freiburg, Dept Ophthalmol, D-79100 Freiburg, Germany
[2] Med Ctr Haaglanden, The Hague, Netherlands
[3] Leicester Royal Infirm, Dept Ophthalmol, Leicester, Leics, England
关键词
D O I
10.1136/bjo.2007.126342
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Aim: To analyse nystagmus characteristics in patients with congenital stationary night blindness (CSNB) for differentiation from other forms of early childhood nystagmus. Methods: Horizontal and vertical eye movements of 10 patients (6 - 46 years, mean 17.1 years, median 12.5 years) with CSNB (eight with CSNB1, two with CSNB2) were recorded with the scleral magnetic search coil technique or by electro-oculography. Nystagmus characteristics such as the amplitude, frequency, conjugacy and intermittency were analysed. Results: All patients had continuous, pendular, oblique and mostly dysconjugate nystagmus of high frequency and low amplitude. In seven cases, a large horizontal or vertical jerk nystagmus with increasing, decreasing or constant velocity was superimposed. Jerk nystagmus was mostly intermittent and conjugate. Head nodding was found not to be compensatory. Conclusions: Eye-movement recordings of CSNB patients disclosed specific nystagmus characteristics, such as an oblique direction, superimposed waveforms and dysconjugate eye movements. These features may help to distinct nystagmus in CSNB from other forms of early infancy nystagmus, such as congenital idiopathic nystagmus, latent nystagmus and spasmus nutans. We found nystagmus in CSNB to be similar to the nystagmus reported in blue-cone monochromatism and rod monochromatism, and in patients with a severe sensory defect. The nystagmus characteristics described should prompt electroretinographic investigation in cases of uncertain diagnosis.
引用
收藏
页码:236 / 240
页数:5
相关论文
共 50 条
  • [41] ROD DENSITOMETRY IN CONGENITAL STATIONARY NIGHT BLINDNESS
    KEUNEN, JEE
    VANMEEL, GJ
    VANNORREN, D
    APPLIED OPTICS, 1988, 27 (06): : 1050 - 1056
  • [42] POSSIBLE PATHOGENESIS OF CONGENITAL STATIONARY NIGHT BLINDNESS
    KATO, M
    AONUMA, H
    KAWAMURA, H
    MIURA, Y
    WATANABE, I
    JAPANESE JOURNAL OF OPHTHALMOLOGY, 1987, 31 (01) : 88 - 101
  • [43] Congenital stationary night blindness in briards in the UK
    Gould, D
    VETERINARY RECORD, 2001, 148 (11) : 351 - 352
  • [44] Congenital stationary night blindness in briards in the UK
    Thomas, R
    Holmes, N
    Binns, M
    VETERINARY RECORD, 2001, 148 (15) : 488 - 488
  • [45] Flash adaptometry in congenital stationary night blindness
    Krastel, H.
    Zyganow, M.
    Mai, M.
    Schlichtenbrede, F.
    ACTA OPHTHALMOLOGICA, 2016, 94
  • [46] ASSIGNMENT OF THE GENE FOR COMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS (CSNB1) TO XP11.3
    MUSARELLA, MA
    WELEBER, RG
    MURPHEY, WH
    YOUNG, RSL
    ANSONCARTWRIGHT, L
    METS, M
    KRAFT, SP
    POLEMENO, R
    LITT, M
    WORTON, RG
    GENOMICS, 1989, 5 (04) : 727 - 737
  • [47] A potential mouse model of incomplete congential stationary night blindness (CSNB2)
    Ball, SL
    Peachey, NS
    Willer, S
    Powers, PA
    Gregg, RG
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (04) : S203 - S203
  • [48] CONGENITAL STATIONARY NIGHT BLINDNESS PRESENTING AS LEBERS CONGENITAL AMAUROSIS
    WELEBER, RG
    TONGUE, AC
    ARCHIVES OF OPHTHALMOLOGY, 1987, 105 (03) : 360 - 365
  • [49] MAPPING OF LOCUS FOR X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS (CSNB1) PROXIMAL TO DXS7
    BECHHANSEN, NT
    MOORE, BJ
    PEARCE, WG
    GENOMICS, 1992, 12 (02) : 409 - 411
  • [50] Characterisation of temporal vision in congenital stationary night blindness
    Ba-Abbad, Rola
    Webster, Andrew
    Moore, Anthony T.
    Michaelides, Michel
    Leroy, Bart Peter
    Stockman, Andrew
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2016, 57 (12)