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‎‏Racemose hemangioma • ‎‏Rare, sporadic phakomatosis that is part of the Wyburn-Mason Syndrome. Clinically presented as arterio-venous malformation (direct A-V communications, with no intervening capillary bed) that can occur in the retina and midbrain. • ‎‏Appear due to vascular dysgenesis of the embryological anterior plexus early in the gestational period, when the primitive vascular mesoderm is shared by the involved structures. • ‎‏Typically unilateral, the ocular symptoms depends on the s
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