Allard R E
J Am Optom Assoc. 1983 Sep;54(9):793-800.
Retinitis pigmentosa is a retinal pigment dystrophy of multiple genetic inheritance patterns affecting approximately .5% of the world population. It may be recognized clinically by observing specific ophthalmoscopic changes, as well as through psychophysical and electrodiagnostic testing. It may also be associated with several other genetic conditions. Basic research indicates that while there is no specific cure, certain precautions may prevent rapid acceleration of the disease process. This article presents an overview of retinitis pigmentosa, including its diagnosis and genetic patterns, and discusses various auxiliary aids and filters that may be helpful in protecting and increasing visual function in R.P. patients.
视网膜色素变性是一种具有多种遗传模式的视网膜色素营养不良,影响着全球约0.5%的人口。临床上可通过观察特定的眼底镜变化以及通过心理物理学和电诊断测试来识别。它也可能与其他几种遗传疾病相关。基础研究表明,虽然没有特效疗法,但某些预防措施可能会防止疾病进程的快速加速。本文概述了视网膜色素变性,包括其诊断和遗传模式,并讨论了各种辅助器具和滤光片,这些可能有助于保护和提高视网膜色素变性患者的视觉功能。