“…DAVMs have been reported to occur in patients with various systemic conditions, particularly syndromes characterised by connective tissue disorders. Potential associations include: atypical Sturge-Weber related syndrome [114], blue rubber-bleb nevus syndrome [115], congenital toxoplasmosis [116], Ehlers-Danlos syndrome [117][118][119], fibromuscular dysplasia [117,120,121], hereditary hemorrhagic telangiectasia [122,123], Marfan's syndrome [124], osteogenesis imperfecta [117], polyarteritis nodosa [125], pseudoxanthoma elasticum [126], Rendu-Osler-Weber syndrome [127], syndactyly [128], and von Recklinghausen's disease [129].…”