Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study

Martins Amelia; Rodrigues Tiago M.; Soares Mario; Dolan Michael-John; Murta Joaquim N.; Silva Rufino; Marques Joao P.

首页> 外文期刊>Graefe's archive for clinical and experimental ophthalmology: Albrecht von Graefes Archiv fur klinische und experimentelle Opthalmologie >Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study

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Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study

机译：围菌和黄斑病态血管血管血管变化术遗传或临床诊断术术术主导视神经萎缩：案例对照研究

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Purpose To evaluate the macular and peripapillary morpho-vascular changes in ADOA, using optical coherence tomography (OCT) and OCT angiography (OCTA).

机译：目的在使用光学相干断层扫描（OCT）和OCT血管造影（OctA）中，评估AdoA的黄斑和围毛状血管变化。

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《Graefe's archive for clinical and experimental ophthalmology: Albrecht von Graefes Archiv fur klinische und experimentelle Opthalmologie》 |2019年第5期|共9页
作者
Martins Amelia; Rodrigues Tiago M.; Soares Mario; Dolan Michael-John; Murta Joaquim N.; Silva Rufino; Marques Joao P.;
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作者单位

CHUC Dept Ophthalmol P-3049 Coimbra Portugal;

CHUC Dept Ophthalmol P-3049 Coimbra Portugal;

CHUC Dept Ophthalmol P-3049 Coimbra Portugal;

Howard Hughes Med Inst Janelia Res Campus Ashburn VA 20147 USA;

CHUC Dept Ophthalmol P-3049 Coimbra Portugal;

CHUC Dept Ophthalmol P-3049 Coimbra Portugal;

CHUC Dept Ophthalmol P-3049 Coimbra Portugal;

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原文格式 PDF
正文语种 eng
中图分类眼科学;
关键词
Autosomal dominant optic atrophy; Morpho-vascular changes; Optical coherence tomography angiography; Radial peripapillary capillary; Parafoveal capillary plexus;

机译：常染色体优势视神经萎缩;语气血管变化;光学相干断层造影血管造影;径向围毛毛细血管毛细血管;Parafoveal毛细血管丛;

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1. Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study [J] . Martins Amelia, Rodrigues Tiago M., Soares Mario, Graefe's archive for clinical and experimental ophthalmology: Albrecht von Graefes Archiv fur klinische und experimentelle Opthalmologie . 2019,第5期

机译：围菌和黄斑病态血管血管血管变化术遗传或临床诊断术术术主导视神经萎缩：案例对照研究
2. High-ResolutionEn FaceImages of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy [J] . KiyokoGocho, SachikoKikuchi, TakenoriKabuto, BioMed research international . 2013,第2期

机译：常染色体显性视神经萎缩患者的微囊性黄斑水肿的高分辨率En FaceImages
3. Clinical and genetic features of eight Chinese autosomal-dominant optic atrophy pedigrees with six novel OPA1 pathogenic variants [J] . Li Huajin, Jones Evan M., Li Hui, Ophthalmic genetics . 2018,第5期

机译：六种新型蛋白质致病性变种八种新型常染色体优势视神经萎缩纤维肽的临床和遗传特征
4. Automatic optic disc segmentation with peripapillary atrophy elimination [C] . Cheng Jun, Liu Jiang, Wong Damon Wing Kee, 33rd Annual International Conference of the IEEE Engineering in Medicine and Biology Society . 2011

机译：椎间盘自动萎缩，消除视神经乳头周围萎缩
5. Experiences of Individuals Adjusting to a Recent Diagnosis of Autosomal Dominant Retinitis Pigmentosa [D] . Satern, Marissa Lauren. 2017

机译：个人适应性常染色体显性视网膜色素变性的最新诊断的经验。
6. High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy [O] . Kiyoko Gocho, Sachiko Kikuchi, Takenori Kabuto, 2006

机译：常染色体显性视神经萎缩患者的微囊性黄斑水肿的高分辨率全脸图像
7. Dominant optic atrophy: correlation between clinical and molecular genetic studies [O] . Anu Puomila, Kirsi Huoponen, Maija Mäntyjärvi, 2005

机译：主导视神经萎缩：临床和分子遗传学研究的相关性

Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study

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