Bilateral central retinal artery occlusions in an infant with hyperhomocysteinemia.

Abstract

A previously healthy 7-week-old boy developed bilateral central retinal artery occlusions in the presence of hyperhomocysteinemia and elevated serum methylmalonic acid and was found to have a transcobalamin receptor mutation. Retinal arterial occlusion is uncommon in young patients and typically prompts a systemic workup. In cases of atypical retinal… (More)
DOI: 10.1016/j.jaapos.2012.04.003

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