Saccadic eye movements in hyperekplexia

被引:9
作者
Tijssen, MAJ
Bollen, E
vanExel, E
vanDijk, JG
机构
[1] Department of Neurology, University Hospital Leiden, Leiden
关键词
hyperekplexia; saccades; brainstem;
D O I
10.1002/mds.870100608
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Hyperekplexia is an autosomal dominant disorder characterized by excessive startle responses followed by a temporary generalized stiffness. The startle response is generated in the medial bulbopontine reticular formation in the lower brainstem. The pulse generator of horizontal saccadic eye movements is localized in the pontine paramedian reticular formation. Measurements of horizontal visually evoked random saccades, antisaccades, and saccades toward remembered targets were performed in seven patients with familial hyperekplexia and seven healthy age-matched controls. The peak velocity of all three kinds of saccades was reduced (p < 0.0001) compared with that of controls. Latencies were marginally longer in the patient group (p = 0.0486). Saccadic gains did not differ between patients and controls. The ability to make antisaccades, saccades toward remembered targets, and the ability to suppress reflex saccades are similar in patients and controls. These data suggest that the origin of the excessive startle response is probably more due to a different modulation in the brainstem than to altered cortical influence.
引用
收藏
页码:749 / 753
页数:5
相关论文
共 12 条
[1]   HORIZONTAL AND VERTICAL SACCADIC EYE-MOVEMENT ABNORMALITIES IN HUNTINGTONS-CHOREA [J].
BOLLEN, E ;
REULEN, JPH ;
DENHEYER, JC ;
VANDERKAMP, W ;
ROOS, RAC ;
BURUMA, OJS .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1986, 74 (01) :11-22
[2]   THE HYPEREKPLEXIAS AND THEIR RELATIONSHIP TO THE NORMAL STARTLE REFLEX [J].
BROWN, P ;
ROTHWELL, JC ;
THOMPSON, PD ;
BRITTON, TC ;
DAY, BL ;
MARSDEN, CD .
BRAIN, 1991, 114 :1903-1928
[3]  
HERISHANU YO, 1981, INVEST OPHTH VIS SCI, V20, P268
[4]   SACCADES IN HUNTINGTONS-DISEASE - INITIATION DEFECTS AND DISTRACTIBILITY [J].
LASKER, AG ;
ZEE, DS ;
HAIN, TC ;
FOLSTEIN, SE ;
SINGER, HS .
NEUROLOGY, 1987, 37 (03) :364-370
[5]   ABNORMAL OCULAR MOTOR CONTROL IN HUNTINGTONS-DISEASE [J].
LEIGH, RJ ;
NEWMAN, SA ;
FOLSTEIN, SE ;
LASKER, AG ;
JENSEN, BA .
NEUROLOGY, 1983, 33 (10) :1268-1275
[6]  
LEIGH RJ, 1991, NEUROLOGY EYE MOVEME, P87
[7]   ANTISACCADES AND REMEMBERED SACCADES IN PARKINSONS-DISEASE [J].
LUECK, CJ ;
TANYERI, S ;
CRAWFORD, TJ ;
HENDERSON, L ;
KENNARD, C .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1990, 53 (04) :284-288
[8]   PHYSIOLOGICAL ABNORMALITIES IN HEREDITARY HYPEREKPLEXIA [J].
MATSUMOTO, J ;
FUHR, P ;
NIGRO, M ;
HALLETT, M .
ANNALS OF NEUROLOGY, 1992, 32 (01) :41-50
[9]   PRECISE RECORDING OF EYE-MOVEMENT - THE IRIS TECHNIQUE .1. [J].
REULEN, JPH ;
MARCUS, JT ;
KOOPS, D ;
DEVRIES, FR ;
TIESINGA, G ;
BOSHUIZEN, K ;
BOS, JE .
MEDICAL & BIOLOGICAL ENGINEERING & COMPUTING, 1988, 26 (01) :20-26
[10]   MUTATIONS IN THE ALPHA-1 SUBUNIT OF THE INHIBITORY GLYCINE RECEPTOR CAUSE THE DOMINANT NEUROLOGIC DISORDER, HYPEREKPLEXIA [J].
SHIANG, R ;
RYAN, SG ;
ZHU, YZ ;
HAHN, AF ;
OCONNELL, P ;
WASMUTH, JJ .
NATURE GENETICS, 1993, 5 (04) :351-358