Therapeutic Approaches for Retinitis Pigmentosa

被引：1

作者：

Pach, J. ^{[1
]}

Gekeler, F. ^{[1
]}

机构：

[1] Univ Klinikum Tubingen, Dept Augenheilkunde, D-72076 Tubingen, Germany

来源：

KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE | 2013年 / 230卷 / 05期

关键词：

retinitis pigmentosa; therapy; gene therapy; neuroprotection; retinal prosthesis; TRANSCORNEAL ELECTRICAL-STIMULATION; SUPRACHOROIDAL-TRANSRETINAL STIMULATION; CILIARY NEUROTROPHIC FACTOR; CONE PHOTORECEPTORS; RETINAL PROSTHESIS; GENE-THERAPY; VISUAL PROSTHESIS; BLIND PATIENTS; ROYAL-COLLEGE; ANIMAL-MODELS;

D O I：

10.1055/s-0032-1328471

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

Background: Retinitis pigmentosa (RP) is a clinically and genetically heterogenous group of hereditary retinal disorders, which lead to progressive loss of vision and finally blindness. Yet there is no approved therapy. Advances in unravelling underlying genetic disorders and pathophysiological mechanisms offer new therapeutic approaches of which some are summarised in this review. Methods: We performed a systematic literature research for defined key words in PubMed. Results: New approaches to therapy for RP include: gene therapy, pharmacological treatment, neuroprotection, electrical stimulation, retinal prostheses, retinal transplantation and optogenetic therapy. Conclusions: Recently there have been advances in new approaches for therapy of dystrophic retinal diseases. Advances in the different approaches are being made at different rates. Although there is no approved therapy yet, the future for treating RP at least in some patients looks promising.

引用

页码：512 / 518

页数：7

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