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角膜内皮营养不良的遗传学

Genetics of corneal endothelial dystrophies.

作者信息

Kannabiran Chitra

机构信息

Kallam Anji Reddy Molecular Genetics Laboratory, Prof Brien Holden Eye Research Centre, L. V. Prasad Eye Institute, Hyderabad, India.

出版信息

J Genet. 2009 Dec;88(4):487-94. doi: 10.1007/s12041-009-0067-1.

Abstract

The corneal endothelium maintains the level of hydration in the cornea. Dysfunction of the endothelium results in excess accumulation of water in the corneal stroma, leading to swelling of the stroma and loss of transparency. There are four different corneal endothelial dystrophies that are hereditary, progressive, non-inflammatory disorders involving dysfunction of the corneal endothelium. Each of the endothelial dystrophies is genetically heterogeneous with different modes of transmission and/or different genes involved in each subtype. Genes responsible for disease have been identified for only a subset of corneal endothelial dystrophies. Knowledge of genes involved and their function in the corneal endothelium can aid understanding the pathogenesis of the disorder as well as reveal pathways that are important for normal functioning of the endothelium.

摘要

角膜内皮维持角膜中的水合水平。内皮功能障碍导致角膜基质中水分过度积聚,导致基质肿胀和透明度丧失。有四种不同的角膜内皮营养不良,它们是遗传性、进行性、非炎症性疾病,涉及角膜内皮功能障碍。每种内皮营养不良在遗传上都是异质性的,具有不同的遗传模式和/或每种亚型中涉及的不同基因。仅在一部分角膜内皮营养不良中鉴定出了致病基因。了解所涉及的基因及其在角膜内皮中的功能有助于理解该疾病的发病机制,并揭示对内皮正常功能很重要的途径。

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