在SSBP1中引起视力缩与视网膜退化的母性马赛克主义:对遗传咨询的含义
Yin-Hsi Chang1,2, Eugene Yu-Chuan Kang1,2,3, Laura Liu1,2
1Department of Ophthalmology, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan, Taiwan.
Orphanet journal of rare diseases
|May 31, 2023
概括
在SSBP1基因中的母性恶体马赛克主义导致光缩-13 (OPA13),一种线粒体疾病. 这一案例凸显了在OPA13诊断和遗传咨询中考虑父母马赛克主义的重要性.
科学领域:
- 遗传学 遗传学 是一个
- 眼科医生 眼科 眼科
- 线粒体疾病 线粒体疾病
背景情况:
- 光学缩-13 (OPA13) 是一种线粒体疾病,其特征是双边光学缩,可能导致视网膜退化.
- OPA13源于SSBP1基因的异构基因突变,导致各种线粒体功能障碍.
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