Pingelapese achromatopsia: correlation between paradoxical pupillary response and clinical features

被引:9
作者
Ben Simon, GJ [1 ]
Abraham, FA [1 ]
Melamed, S [1 ]
机构
[1] Chaim Sheba Med Ctr, Goldschleger Eye Inst, IL-52621 Tel Hashomer, Israel
关键词
D O I
10.1136/bjo.2003.027284
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Aim: To evaluate the paradoxical pupillary constriction in darkness in patients with Pingelapese achromatopsia (PA), and to describe a connection between this phenomenon and the clinical features. Methods: 27 patients with PA were examined. All underwent a full ophthalmic examination which included Snellen visual acuity and ophthalmoscopy. Colour vision examination was performed with Ishihara pseudoisochromatic plates and also with a colour plate consisting of five basic colours ( red, green, purple, yellow, and orange). Paradoxical pupillary response was examined and documented with a special infrared video camera. Pupils' images were analysed using the Scion Image program and the ratio of pupil size in darkness to its size in light was calculated and recorded. Results: Mean visual acuity was 20/400 ( range 20/80-20/ 800). Colour vision examination showed a mean of 3.2 (SD 1.5) ( range 1 - 5) of Ishihara colour plates, and 0.5 (0.75) ( 0 3) of basic colour plates. 23 patients (85%) had paradoxical pupillary constriction in darkness. Mean dark/light ratio of pupillary area was 0.86 ( range 0.5 - 1.6). In patients with marked paradoxical pupillary constriction there was a significant correlation of visual acuity and Ishihara score. Conclusions: Clinical manifestations of achromatopsia include total colour blindness, low visual acuity ( mean of 20/400), horizontal pendular or rotatory nystagmus, and photophobia. Most patients have paradoxical pupillary constriction in darkness. When this response is brisk it seems to correlate with lower visual acuity and lower Ishihara score.
引用
收藏
页码:223 / 225
页数:3
相关论文
共 19 条
[1]   Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling [J].
Arbour, NC ;
Zlotogora, J ;
Knowlton, RG ;
Merin, S ;
Rosenmann, A ;
Kanis, AB ;
Rokhlina, T ;
Stone, EM ;
Sheffield, VC .
HUMAN MOLECULAR GENETICS, 1997, 6 (05) :689-694
[2]  
BARRICKS ME, 1977, ARCH OPHTHALMOL-CHIC, V95, P1800
[3]  
BRODY JA, 1970, LANCET, V1, P1253
[4]   ACHROMATOPSIA IN PINGELAP ISLANDERS - STUDY OF A GENETIC ISOLATE [J].
CARR, RE ;
MORTON, NE ;
SIEGEL, IM .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1971, 72 (04) :746-&
[5]   PARADOXICAL PUPIL IN CONGENITAL ACHROMATOPSIA [J].
FLYNN, JT ;
KAZARIAN, E ;
BARRICKS, M .
INTERNATIONAL OPHTHALMOLOGY, 1981, 3 (02) :91-96
[6]  
FRANCOIS J, 1961, HEREDITY OPHTHALMOLO, P198
[7]  
HUSSELS IE, 1972, AM J HUM GENET, V24, P304
[8]  
JACOBSON DM, 1989, OPHTHALMOLOGY, V96, P885
[9]  
JAGER W, 1972, HDB SENSORY PHYSL, P625
[10]   Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel [J].
Kohl, S ;
Marx, T ;
Giddings, I ;
Jägle, H ;
Jacobson, SG ;
Apfelstedt-Sylla, E ;
Zrenner, E ;
Sharpe, LT ;
Wissinger, B .
NATURE GENETICS, 1998, 19 (03) :257-259