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霍纳综合征:人类虹膜的电子显微镜研究

Horner's syndrome: an electron microscopic study of a human iris.

作者信息

McCartney A C, Riordan-Eva P, Howes R C, Spalton D J

机构信息

Institute of Ophthalmology, London.

出版信息

Br J Ophthalmol. 1992 Dec;76(12):746-9. doi: 10.1136/bjo.76.12.746.

Abstract

Electron microscopy was performed on the irides of a man with a history of a long standing Horner's syndrome which resulted in iris heterochromia. Comparison of his normal brown iris with the depigmented blue iris showed depletion of anterior border cells and absence of sympathetic nerve fibres. Stromal melanocyte numbers were also diminished but melanosome numbers within the residual cells were not significantly different. Postnatal maintenance of stromal and anterior border zone pigmentation, derived from the neural crest, would appear to be dependent on an intact sympathetic nerve supply in contrast to the iris pigment epithelium which remains normally unaffected in Horner's syndrome.

摘要

对一名有长期霍纳综合征病史并导致虹膜异色的男性的虹膜进行了电子显微镜检查。将他正常的棕色虹膜与色素脱失的蓝色虹膜进行比较,结果显示前缘细胞减少且交感神经纤维缺失。基质黑素细胞数量也减少,但残留细胞内的黑素体数量没有显著差异。与虹膜色素上皮在霍纳综合征中通常不受影响不同,源自神经嵴的基质和前缘区色素沉着的出生后维持似乎依赖于完整的交感神经供应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0f7/504397/cc795e7e872a/brjopthal00060-0043-a.jpg

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