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Leber's congenital amaurosis.

作者信息

Mizuno K, Takei Y, Sears M L, Peterson W S, Carr R E, Jampol L M

出版信息

Am J Ophthalmol. 1977 Jan;83(1):32-42. doi: 10.1016/0002-9394(77)90188-x.

DOI:10.1016/0002-9394(77)90188-x
PMID:835664
Abstract

An early stage of Leber's congenital amaurosis, characterized by white spots or lines in the fundus, occurred in two children. Light microscopic examination of eyes obtained from one child, a 16-month-old Japanese girl, revealed subretinal deposits corresponding to the white spots and lines in the fundus deposits. Light and electron microscopic examination of the eye showed distinctive changes in the outer retinal layers and choroid, while the inner retinal layers were nearly normal. Characteristic early lesions of congenital amaurosis appeared to be produced by deposits consisting of loose outer segments and apical processes of the pigmental epithelial cell and macrophages. Undifferentiation in the nuclei of the photoreceptor cell, the inner segment, the pigment epithelial cell, and the choriocapillaris were likely characteristics of the early changes of congenital amaurosis.

摘要

相似文献

1
Leber's congenital amaurosis.
Am J Ophthalmol. 1977 Jan;83(1):32-42. doi: 10.1016/0002-9394(77)90188-x.
2
Leber's congenital amaurosis. A retrospective study of 33 cases and a histopathological study of one case.莱伯先天性黑蒙。33例回顾性研究及1例组织病理学研究。
Arch Ophthalmol. 1978 May;96(5):818-21. doi: 10.1001/archopht.1978.03910050424004.
3
Clinical spectrum of leber's congenital amaurosis in the second to fourth decades of life.莱伯先天性黑矇在人生第二个至第四个十年的临床谱。
Ophthalmology. 1990 Sep;97(9):1156-61. doi: 10.1016/s0161-6420(90)32442-9.
4
[Leber's congenital amaurosis].
Rev Chir Oncol Radiol O R L Oftalmol Stomatol Ser Oftalmol. 1986 Apr-Jun;30(2):119-23.
5
Follow-up and diagnostic reappraisal of 75 patients with Leber's congenital amaurosis.75例莱伯先天性黑矇患者的随访及诊断重新评估
Am J Ophthalmol. 1989 Jun 15;107(6):624-31. doi: 10.1016/0002-9394(89)90259-6.
6
Leber's congenital amaurosis as conceived by Leber.
Ophthalmologica. 1979;179(1):48-51. doi: 10.1159/000308863.
7
A pedigree of Leber's congenital amaurosis.莱伯先天性黑蒙的系谱图。
Ophthalmic Paediatr Genet. 1988 Mar;9(1):29-36. doi: 10.3109/13816818809031478.
8
The ocular pathology in Leber's congenital amaurosis.莱伯先天性黑矇的眼部病理学
Aust N Z J Ophthalmol. 1994 Feb;22(1):25-31. doi: 10.1111/j.1442-9071.1994.tb01691.x.
9
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).视网膜变性12(rd12):一种新的、自发产生的人类莱伯先天性黑蒙(LCA)小鼠模型。
Mol Vis. 2005 Feb 28;11:152-62.
10
Leber's congenital amaurosis with marbelized fundus and juvenile nephronophthisis.伴有眼底大理石样改变的莱伯先天性黑矇和青少年肾单位肾痨。
Am J Ophthalmol. 1989 Apr 15;107(4):426-8. doi: 10.1016/0002-9394(89)90670-3.

引用本文的文献

1
Late presentation of RPE65 retinopathy in three siblings.三名兄弟姐妹中RPE65视网膜病变的延迟表现。
Doc Ophthalmol. 2020 Jun;140(3):289-297. doi: 10.1007/s10633-019-09745-z. Epub 2020 Jan 10.
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Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy.由 RPE65 突变引起的莱伯先天性黑蒙症及其基因治疗。
Prog Retin Eye Res. 2010 Sep;29(5):398-427. doi: 10.1016/j.preteyeres.2010.04.002. Epub 2010 Apr 24.
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Differential macular morphology in patients with RPE65-, CEP290-, GUCY2D-, and AIPL1-related Leber congenital amaurosis.
RPE65、CEP290、GUCY2D 和 AIPL1 相关莱伯先天性黑矇患者的黄斑形态差异。
Invest Ophthalmol Vis Sci. 2010 May;51(5):2608-14. doi: 10.1167/iovs.09-3734. Epub 2009 Dec 3.
4
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13.莱伯先天性黑蒙(LCA)的遗传异质性证据及LCA1基因定位于染色体17p13
Hum Genet. 1996 Jun;97(6):798-801. doi: 10.1007/BF02346192.
5
Senior-Løken syndrome with marbelized fundus and unusual skeletal abnormalities. A case report.伴有眼底大理石样改变及特殊骨骼异常的Senior-Løken综合征。病例报告。
Graefes Arch Clin Exp Ophthalmol. 1993 Apr;231(4):242-6. doi: 10.1007/BF00918849.
6
Yellowish flecks in Leber's congenital amaurosis.莱伯先天性黑矇中的淡黄色斑点。
Br J Ophthalmol. 1984 Oct;68(10):727-31. doi: 10.1136/bjo.68.10.727.
7
Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation.伴有视网膜发育异常的儒贝尔综合征:以新生儿呼吸急促为线索的一种遗传性脑眼畸形
Arch Dis Child. 1984 Aug;59(8):709-18. doi: 10.1136/adc.59.8.709.