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2023 | 1 |
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Current Management Options for Patients with Retinitis Pigmentosa.
Methods Mol Biol. 2023;2560:353-361. doi: 10.1007/978-1-0716-2651-1_32.
Methods Mol Biol. 2023.
PMID: 36481910
With an estimated prevalence of 1 in 4000 worldwide [1], retinitis pigmentosa (RP) comprises a spectrum of progressive inherited retinal disorders that can lead to blindness as early as age 30 [2]. ...Herein, this chapter will discuss the therapeuti …
With an estimated prevalence of 1 in 4000 worldwide [1], retinitis pigmentosa (RP) comprises a spectrum of progr …
Characterizing the phenotype and genotype of a family with occult macular dystrophy.
Chen CJ, Scholl HP, Birch DG, Iwata T, Miller NR, Goldberg MF.
Chen CJ, et al.
Arch Ophthalmol. 2012 Dec;130(12):1554-9. doi: 10.1001/archophthalmol.2012.2683.
Arch Ophthalmol. 2012.
PMID: 23229695
Free PMC article.
Occult macular dystrophy is a rare macular dystrophy with central cone dysfunction hidden behind a normal fundus appearance that has been attributed to a mutation in the retinitis pigmentosa 1-like 1 (RP1L1) gene in 4 Japanese families. METHODS: In thi …
Occult macular dystrophy is a rare macular dystrophy with central cone dysfunction hidden behind a normal fundus appearance that has been at …
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