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Prominent choroidal atrophy is a feature of multiple inherited retinal disorders with choroideremia as the classic and most commonly encountered example. In this chapter, we review the genetic and clinical features of choroideremia, gyrate atrophy, and other hereditary conditions manifesting with choroidal atrophy with discussions of underlying mechanisms and potential therapies as relevant.

More information Original publication

DOI

10.1007/978-3-030-42634-7_4

Type

Chapter

Publication Date

2022-01-01T00:00:00+00:00

Pages

3997 - 4012

Total pages

15