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Meesmann's epithelial dystrophy of the cornea.

作者信息

Fine B S, Yanoff M, Pitts E, Slaughter F D

出版信息

Am J Ophthalmol. 1977 May;83(5):633-42. doi: 10.1016/0002-9394(77)90128-3.

DOI:10.1016/0002-9394(77)90128-3
PMID:301357
Abstract

Two separate pedigrees had typical Meesmann's dystrophy of the corneal epithelium. Histologic examination of one patient from each pedigree showed two characteristic findings in corneal epithelium; the previously designated "peculiar substance" in the cells, and the vacuolated homogeneous substance mostly within the cysts. The primary disturbance probably involves the cytoplasmic ground substance that ultimately may result in complete homogenization of cells and the formation of cysts. Thickening of the epithelial basement membrane is variable and is a nonspecific response by the epithelial basal cells.

摘要

相似文献

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Meesmann's epithelial dystrophy of the cornea.
Am J Ophthalmol. 1977 May;83(5):633-42. doi: 10.1016/0002-9394(77)90128-3.
2
Meesmann's corneal dystrophy: ultrastructural features.
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Meesmann's epithelial dystrophy of the cornea. Biometrics and a hypothesis.米斯曼角膜上皮营养不良。生物统计学与一种假说。
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A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy.与米斯曼上皮性角膜营养不良相关的角蛋白12新突变。
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Clinicopathologic case report: ultrastructure of the epithelial dystrophy of Meesmann.
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8
Unilateral Meesmann's dystrophy.
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9
Microcystic dystrophy of the cornea. A partial explanation for its pathogenesis.角膜微囊性营养不良。对其发病机制的部分解释。
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10
Microcystic corneal dystrophy.微囊状角膜营养不良
Trans Am Ophthalmol Soc. 1976;74:488-531.

引用本文的文献

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A Novel Pathogenic Variant in the Gene in a Family with Meesmann Corneal Dystrophy.患有米斯曼角膜营养不良的一个家族中该基因的一种新型致病变异。
J Clin Med. 2025 Jan 28;14(3):851. doi: 10.3390/jcm14030851.
2
In vivo histology and p.L132V mutation in KRT12 gene in Japanese patients with Meesmann corneal dystrophy.日本米斯曼角膜营养不良患者的体内组织学及角蛋白12基因p.L132V突变
Jpn J Ophthalmol. 2019 Jan;63(1):46-55. doi: 10.1007/s10384-018-00643-6. Epub 2018 Dec 7.
3
Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy.
角蛋白12错义突变在米斯曼上皮性角膜营养不良中诱导未折叠蛋白反应和细胞凋亡。
Hum Mol Genet. 2016 Mar 15;25(6):1176-91. doi: 10.1093/hmg/ddw001. Epub 2016 Jan 11.
4
Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.严重的米斯曼氏上皮性角膜营养不良表型归因于角蛋白 12 的螺旋起始基序中的错义突变。
Eye (Lond). 2013 Mar;27(3):367-73. doi: 10.1038/eye.2012.261. Epub 2012 Dec 7.
5
Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann's corneal dystrophy in a German family.在一个德国家庭中鉴定出角膜特异性角蛋白12基因的一种新突变,该突变导致米斯曼角膜营养不良。
Mol Vis. 2010 May 29;16:954-60.
6
The IC3D classification of the corneal dystrophies.角膜营养不良的IC3D分类
Cornea. 2008 Dec;27 Suppl 2(Suppl 2):S1-83. doi: 10.1097/ICO.0b013e31817780fb.
7
Corneal dystrophies.角膜营养不良
Orphanet J Rare Dis. 2009 Feb 23;4:7. doi: 10.1186/1750-1172-4-7.
8
A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy.米斯曼角膜营养不良中角膜特异性角蛋白12基因的一种新突变。
Jpn J Ophthalmol. 2008 May-Jun;52(3):224-226. doi: 10.1007/s10384-007-0518-2. Epub 2008 Jul 27.
9
A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.一种导致米斯曼角膜营养不良严重表型的角蛋白12基因新突变。
Mol Vis. 2007 Jun 21;13:975-80.
10
A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy.角蛋白12基因1A结构域的一种新型精氨酸替代突变及2B结构域的一种新型27bp插入突变与米斯曼角膜营养不良相关。
Br J Ophthalmol. 2004 Jun;88(6):752-6. doi: 10.1136/bjo.2003.032870.