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PedAM

Pediatric Disease Annotations & Medicines




Disease hereditary hemorrhagic telangiectasia
Phenotype C0006123|branch retinal artery occlusion
Sentences 1
PubMedID- 25372443 Purpose: to describe a case of hereditary hemorrhagic telangiectasia, presenting with multiple branch retinal artery occlusions, retinal ischemia, neovascularization, and vitreous hemorrhage after cerebral arteriovenous malformation embolization.

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