OCULAR MANIFESTATIONS OF COCKAYNES SYNDROME

被引:26
作者
COLES, WH
机构
[1] Department of Ophthalmology, Louisiana State University School of Medicine New Orleans, LA
关键词
D O I
10.1016/S0002-9394(69)91006-X
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Cockayne's syndrome is a rare inherited disorder characterized ophthalmoscopically by retinal pigmentary degeneration, optic atrophy and arteriolar narrowing. In addition, the two brothers with Cockayne's syndrome reported here showed corneal opacification, exotropia and photophobia. © 1969.
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页码:762 / &
相关论文
共 9 条
[1]  
Cockayne E A, 1936, Arch Dis Child, V11, P1
[2]   DWARFISM WITH RETINAL ATROPHY AND DEAFNESS [J].
COCKAYNE, EA .
ARCHIVES OF DISEASE IN CHILDHOOD, 1946, 21 (105) :52-54
[3]  
LEIBERMAN WJ, 1961, AM J OPHTH, V52, P116
[4]  
MACDONALD W B, 1960, Pediatrics, V25, P997
[5]   A SYNDROME RESEMBLING PROGERIA - A REVIEW OF 2 CASES [J].
NEILL, CA ;
DINGWALL, MM .
ARCHIVES OF DISEASE IN CHILDHOOD, 1950, 25 (123) :213-223
[6]  
PADDISON RM, 1963, DERMATOL TROPICA, V2, P195
[7]  
WALSH FB, 1957, CLIN NEURO OPHTH, P646
[8]  
WILKINS L, 1965, DIAGNOSIS TREATMENT, P168
[9]  
WILKINS L, 1965, DIAGNOSIS TREATMENT, P192