Peripheral Retinal Nonperfusion in Septo-optic Dysplasia (de Morsier Syndrome) | Zendy

Daniel F. Kiernan | Zendy; Omar Al-Heeti | Zendy; Michael P. Blair | Zendy; Jeremy D. Keenan | Zendy; Steven J. Lichtenstein | Zendy; Ekaterini Tsilou | Zendy; Nizar Smaoui | Zendy; Michael J. Shapiro | Zendy

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Peripheral Retinal Nonperfusion in Septo-optic Dysplasia (de Morsier Syndrome)

Author(s) -

Daniel F. Kiernan,

Omar Al-Heeti,

Michael P. Blair,

Jeremy D. Keenan,

Steven J. Lichtenstein,

Ekaterini Tsilou,

Nizar Smaoui,

Michael J. Shapiro

Publication year - 2011

Publication title -

archives of ophthalmology

Language(s) - English

Resource type - Journals

eISSN - 1538-3601

pISSN - 0003-9950

DOI - 10.1001/archophthalmol.2011.92

Subject(s) - medicine , ophthalmology , peripheral , retinal , dysplasia , pathology

tocoagulation was applied and the worm was successfully killed (Figure 1F). The patient reported significant subjective improvement, and his visual acuity measured 20/40 OS 1 month and 20/25 OS 3 months following the initial visit. Spectraldomain OCT showed disruption of the photoreceptors in the papillomacular region secondary to prior photocoagulation but progressive restoration of the normal inner segment/outer segment junction and photoreceptor architecture in the fovea (Figure 2B and C).

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