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Meesmann's corneal dystrophy: ultrastructural features.

作者信息

Tremblay M, Dubé I

出版信息

Can J Ophthalmol. 1982 Feb;17(1):24-8.

PMID:6979375
Abstract

Ultrastructural studies were done on a cornea obtained at the time of lamellar keratoplasty from a patient with the clinical diagnosis of Meesmann's corneal dystrophy. Light microscopy showed in the corneal epithelium the typical tiny cysts containing cellular debris and a homogeneous substance that reacted with periodic acid and Schiff's reagent and stained with Hale's colloidal iron; as well, the basement membrane was markedly thickened. Electron microscopy revealed that the cysts had a corrugated or microvillous wall, consistent with acantholysis. The epithelial cells were rich in glycogen, and many contained the peculiar substance described by others in Meesmann's corneal dystrophy. This substance appeared to be derived from the tonofilaments and was in close relation to the desmosomes. The thick basement membrane showed secondary changes, with one thick zone that was rich in collagen fibrils mimicking abnormal anchoring fibrils and one thin zone that was poor in fibrils but had frequent intercalated fibroblasts and probably represented a repair phenomenon. There was no apparent modification of Bowman's layer or the superficial stroma.

摘要

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引用本文的文献

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2
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。
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A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.
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Mol Vis. 2007 Jun 21;13:975-80.
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Br J Ophthalmol. 2002 Jul;86(7):729-32. doi: 10.1136/bjo.86.7.729.
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A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy.德国一个患有米斯曼角膜营养不良家族中的一种新型角蛋白12突变。
Br J Ophthalmol. 2000 May;84(5):527-30. doi: 10.1136/bjo.84.5.527.
6
Unilateral Meesmann's dystrophy.
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