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Article
November 1994

Retinopathy Associated With Hemoglobin AC

Author Affiliations

Baltimore, Md

Arch Ophthalmol. 1994;112(11):1410-1411. doi:10.1001/archopht.1994.01090230024010
Abstract

Peripheral retinal neovascularization is a well-studied complication of sickle cell hemoglobinopathy and has been recognized in hemoglobin SC disease, hemoglobin SS disease, and sickle cell—β-thalassemia and occasionally in hemoglobin AS disease (sickle cell trait).1 There are only a few reports in the literature of retinal vascular changes associated with hemoglobin AC disease (C trait),1-3 a condition that generally has limited clinical manifestations. We report herein a case of subhyaloid hemorrhage and peripheral retinal neovascularization in the setting of hemoglobin AC disease.

Report of a Case.  A 57-year-old black man with a history of systemic hypertension and coronary artery disease presented in April 1988 with a complaint of central scotoma in the left eye. Best corrected visual acuities were 20/20 OD and 20/400 OS, and the findings on slit-lamp examination were normal in both eyes. Ophthalmoscopic examination of the right eye revealed a few, small, peripheral intraretinal hemorrhages. Ophthalmoscopic

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