Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature
Conclusion:
Observation of RPE abnormalities in the context of suggestive systemic findings should prompt mtDNA testing.
Source: BMC Ophthalmology - Latest articles - Category: Opthalmology Authors: Alejandra DaruichAlexandre MatetFrançois-Xavier Borruat Source Type: research
More News: Anatomy | Angiography | Audiology | Chronic Fatigue Syndrome | Chronic Pain | Deafness | Diabetes | Diabetes Mellitus | Endocrinology | Eyes | Genetics | Headache | Migraine | Opthalmology | Pain | Reflex Sympathetic Dystrophy | Stroke