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 21 条
  • [1] ABADI RV, 1986, DOC OPHTHALMOL, V64, P153, DOI 10.1007/BF00159990
  • [2] Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
    Bech-Hansen, NT
    Naylor, MJ
    Maybaum, TA
    Sparkes, RL
    Koop, B
    Birch, DG
    Bergen, AAB
    Prinsen, CFM
    Polomeno, RC
    Gal, A
    Drack, AV
    Musarella, MA
    Jacobson, SG
    Young, RSL
    Weleber, RG
    [J]. NATURE GENETICS, 2000, 26 (03) : 319 - 323
  • [3] Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
    Bech-Hansen, NT
    Naylor, MJ
    Maybaum, TA
    Pearce, WG
    Koop, B
    Fishman, GA
    Mets, M
    Musarella, MA
    Boycott, KM
    [J]. NATURE GENETICS, 1998, 19 (03) : 264 - 267
  • [4] Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F
    Boycott, KM
    Pearce, WG
    Bech-Hansen, NT
    [J]. CANADIAN JOURNAL OF OPHTHALMOLOGY-JOURNAL CANADIEN D OPHTALMOLOGIE, 2000, 35 (04): : 204 - 213
  • [5] A comparison of ERG abnormalities in XLRS and XLCSNB
    Bradshaw, K
    Allen, L
    Trump, D
    Hardcastle, A
    George, N
    Moore, A
    [J]. DOCUMENTA OPHTHALMOLOGICA, 2004, 108 (02) : 135 - 145
  • [6] CONGENITAL NYSTAGMUS WAVEFORMS AND FOVEATION STRATEGY
    DELLOSSO, LF
    DAROFF, RB
    [J]. DOCUMENTA OPHTHALMOLOGICA, 1975, 39 (01) : 155 - 182
  • [7] DELLOSSO LF, 1979, ARCH OPHTHALMOL-CHIC, V97, P1877
  • [8] GOTTLOB I, 1992, OPHTHALMOLOGY, V99, P1024
  • [9] GOTTLOB I, 1990, OPHTHALMOLOGY, V97, P1166
  • [10] QUANTITATIVE EYE AND HEAD MOVEMENT RECORDINGS OF RETINAL DISEASE MIMICKING SPASMUS NUTANS
    GOTTLOB, I
    WIZOV, SS
    REINECKE, RD
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1995, 119 (03) : 374 - 376