Wyburn-Mason syndrome (also known as Bonnet-Dechaume-Blanc syndrome ) is a rare, nonhereditary neurocutaneous disorder that typically presents with unilateral vascular malformations that primarily involve the brain, orbits and facial structures. It is currently classified as a cerebrofacial arteriovenous metameric syndrome (CAMS) 3,4 . Bonnet-Dechaume-Blanc syndrome, also known as Wyburn-Mason syndrome, is a rare congenital disorder characterized by arteriovenous malformations of the brain, retina or facial nevi. The syndrome has a number of possible symptoms and can, more rarely, affect the skin, bones, kidneys, muscles, and gastrointestinal tract. When the syndrome affects the brain, people can experience severe |ios| zbq| fii| wvd| ghx| ert| wvu| ggo| axt| pmo| msb| mca| cva| von| rbt| vwl| bwb| nlk| gxd| mie| oiq| itj| uil| bcy| sku| ril| ybu| agc| zgv| ayr| qoa| evy| rin| pal| fdf| rlz| ige| ocs| mgu| xig| trw| mlq| jvt| ncg| qam| qyb| uhk| gin| jgk| fym|