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Usher's syndrome, temporal bone pathology.

作者信息

Cremers C W, Delleman W J

机构信息

Department of Otorhinolaryngology, University of Nijmegen, The Netherlands.

出版信息

Int J Pediatr Otorhinolaryngol. 1988 Oct;16(1):23-30. doi: 10.1016/0165-5876(88)90096-1.

DOI:10.1016/0165-5876(88)90096-1
PMID:3203983
Abstract

The histological findings in the right temporal bone of a 65-year-old deaf and blind man are presented. The subject suffered from the autosomal recessive Usher's syndrome, as did 2 of his 5 siblings. They are the offspring of a consanguineous marriage. This man died from an intra-abdominal hemorrhage. Within 3 h after death the temporal bones were donated for study and were processed for histopathological examination.

摘要

相似文献

1
Usher's syndrome, temporal bone pathology.
Int J Pediatr Otorhinolaryngol. 1988 Oct;16(1):23-30. doi: 10.1016/0165-5876(88)90096-1.
2
Usher's syndrome. (Retinitis pigmentosa and deafness). A temporal bone report.尤塞综合征(色素性视网膜炎和耳聋)。一份颞骨报告。
J Laryngol Otol. 1975 Feb;89(2):175-81. doi: 10.1017/s0022215100080233.
3
An evaluation of genetic carriers of Usher's syndrome.对乌舍尔综合征基因携带者的评估。
Am J Ophthalmol. 1972 Nov;74(5):940-7. doi: 10.1016/0002-9394(72)91215-9.
4
[Cochleo-vestibular manifestations in retinitis pigmentosa (Usher's syndrome)].[色素性视网膜炎(尤塞综合征)中的耳蜗-前庭表现]
Acta Otorinolaryngol Iber Am. 1972;23(4):517-24.
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Clinical variation in Usher's syndrome.遗传性耳聋-视网膜色素变性综合征的临床变异
Arch Otolaryngol. 1971 Oct;94(4):321-34. doi: 10.1001/archotol.1971.00770070513007.
6
[Present conception of Usher's syndrome].[关于乌舍尔综合征的当前概念]
Rev Otoneuroophtalmol. 1970 Nov;42(7):422-5.
7
Usher's syndrome--a premium on prevention.乌舍尔综合征——预防的重中之重。
Sight Sav Rev. 1969 Fall;39(3):152.
8
[Usher's syndrome. Description of 3 cases].[乌舍尔综合征。3例病例描述]
Bull Mem Soc Fr Ophtalmol. 1969;82:147-51.
9
Usher's syndrome--deafness and progressive blindness. Clinical cases, prevention, theory and literature survey.
J Chronic Dis. 1969 Aug;22(3):133-51. doi: 10.1016/0021-9681(69)90055-1.
10
[Usher's syndrome (association of familial pigmented retinopathy and deafness) 2 cases in a family].[乌舍尔综合征(家族性色素性视网膜病变与耳聋的关联):一家族中有2例]
Pediatrie. 1968 Dec;23(8):948-51.

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Cochlear histopathology in human genetic hearing loss: State of the science and future prospects.人类遗传性听力损失的耳蜗组织病理学:科学现状和未来展望。
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Genetic screening revealed usher syndrome in a paediatric Chinese patient.
基因筛查显示一名中国儿科患者患有尤塞综合征。
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