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Quoted phrase not found in phrase index: "Nummular pigmentation of the fundus"
Page 1
Vogt-Koyanagi-Harada Syndrome in Brazilian Children.
Marquezan MC, Nascimento H, Dalbem D, Muccioli C, Belfort R. Marquezan MC, et al. Ocul Immunol Inflamm. 2020 Apr 2;28(3):402-408. doi: 10.1080/09273948.2019.1588982. Epub 2019 May 23. Ocul Immunol Inflamm. 2020. PMID: 31120768
The patients, who ranged in age from 5 to 8 years, all presented with chronic disease. The most common ocular finding was abnormal fundus pigmentation in five patients followed by band keratopathy in four. ...
The patients, who ranged in age from 5 to 8 years, all presented with chronic disease. The most common ocular finding was abnormal fundus …
Enhanced S-cone syndrome: Clinical spectrum in Indian population.
Naik A, Ratra D, Banerjee A, Dalan D, Jandyal S, Rao G, Sen P, Bhende M, Jayaprakash V, Susvar P, Walinjkar J, Rao C. Naik A, et al. Indian J Ophthalmol. 2019 Apr;67(4):523-529. doi: 10.4103/ijo.IJO_1480_18. Indian J Ophthalmol. 2019. PMID: 30900587 Free PMC article.
The disease presented in the 1(st) decade with night blindness and was almost stationary or minimally progressive. Mid-peripheral fundus changes in form of nummular pigmentary alterations, yellow punctate lesions, and macular schisis were noted. ...CONCLUSION: ESCS …
The disease presented in the 1(st) decade with night blindness and was almost stationary or minimally progressive. Mid-peripheral fundus …
Enhanced S-Cone Syndrome: Spectrum of Clinical, Imaging, Electrophysiologic, and Genetic Findings in a Retrospective Case Series of 56 Patients.
de Carvalho ER, Robson AG, Arno G, Boon CJF, Webster AA, Michaelides M. de Carvalho ER, et al. Ophthalmol Retina. 2021 Feb;5(2):195-214. doi: 10.1016/j.oret.2020.07.008. Epub 2020 Jul 15. Ophthalmol Retina. 2021. PMID: 32679203 Free PMC article.
PURPOSE: To describe the detailed phenotype, long-term clinical course, clinical variability, and genotype of patients with enhanced S-cone syndrome (ESCS). ...Clinical findings were highly variable and included foveomacular schisis (41.1% [26/56]), yellow-white dots (57.1 …
PURPOSE: To describe the detailed phenotype, long-term clinical course, clinical variability, and genotype of patients with enhanced …
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.
Henderson RH, Mackay DS, Li Z, Moradi P, Sergouniotis P, Russell-Eggitt I, Thompson DA, Robson AG, Holder GE, Webster AR, Moore AT. Henderson RH, et al. Br J Ophthalmol. 2011 Jun;95(6):811-7. doi: 10.1136/bjo.2010.186882. Epub 2010 Oct 17. Br J Ophthalmol. 2011. PMID: 20956273
METHODS: A detailed clinical examination was performed, including: logMAR visual acuity, refraction, Goldmann visual fields, slit-lamp biomicroscopy, fundus photography, autofluorescence imaging and optical coherence tomography. ...Common phenotypic features included hyper …
METHODS: A detailed clinical examination was performed, including: logMAR visual acuity, refraction, Goldmann visual fields, slit-lamp biomi …
Cancer-associated nummular loss of the retinal pigment epithelium.
Lee JM, Seong HK, Nam WH, Kim HK. Lee JM, et al. Korean J Ophthalmol. 2007 Dec;21(4):261-4. doi: 10.3341/kjo.2007.21.4.261. Korean J Ophthalmol. 2007. PMID: 18063894 Free PMC article.
PURPOSE: To report a case of cancer-associated nummular loss of the retinal pigment epithelium. METHODS: A 47-year-old man with a history of hepatocellular carcinoma presented with three weeks of bilateral visual loss. ...CONCLUSIONS: We report a case of visual para …
PURPOSE: To report a case of cancer-associated nummular loss of the retinal pigment epithelium. METHODS: A 47-year-old man wit …