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单基因青光眼的临床实践指南
引用本文:无,杨正林,杨季云,龚波,张清炯. 单基因青光眼的临床实践指南[J]. 中华医学遗传学杂志, 2020, 0(3): 329-333
作者姓名:  杨正林  杨季云  龚波  张清炯
作者单位:中华医学会医学遗传学分会遗传病临床实践指南撰写组;电子科技大学医学院、电子科技大学附属医院·四川省人民医院人类疾病基因研究重点实验室;中山大学中山眼科中心
摘    要:青光眼(glaucoma)是一组视网膜神经节细胞及其轴突变性的进行性视神经病,其典型临床特征为视乳头凹陷性萎缩和特征性视野缺损,遗传因素在其发病过程中起着重要作用。本指南主要介绍单基因变异相关的青光眼,包括原发性先天性青光眼(primary congenital glaucom a,PCG)和原发性开角型青光眼(primary open-angle glaucoma,POAG)的致病基因、疾病诊断以及临床咨询等方面,旨在规范单基因青光眼临床分子遗传诊疗,为临床医生对单基因青光眼诊治和遗传咨询服务提供参考。

关 键 词:原发性先天性青光眼  原发性开角型青光眼  分子诊断  指南

Clinical practice guidelines for single gene glaucoma disorder
无,Yung Zhenglin,Yang Jiyun,Gong Bo,Zhang Qingjiong. Clinical practice guidelines for single gene glaucoma disorder[J]. Chinese journal of medical genetics, 2020, 0(3): 329-333
Authors:  Yung Zhenglin  Yang Jiyun  Gong Bo  Zhang Qingjiong
Affiliation:(Writing Group for Practice Guidelines for Diagnosis and Treatment of Genetic Diseases,Medical Genetics Branch of Chinese Medical Association;不详)
Abstract:Glaucoma is a group of progressive optic neuropathies featuring retinal ganglion cell and axonal degeneration,which typically manifest as sunken atrophy of optic papilla and characteristic visual field defect.Genetic factors play an important role in the pathogenesis of glaucoma.This guideline mainly focuses on single gene mutation-related glaucoma by summarizing the pathogenic genes,disease diagnosis and clinical consultation of primary congenital glaucoma(PCG)and primary open-angle glaucoma(POAG),with an aim to regulate their molecular diagnosis,genetic counseling and treatment.
Keywords:Primary congenital glaucoma  Primary open-angle glaucoma  Molecular diagnosis  Practical guideline
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