Weber syndrome due to penetrating wound in midbrain. Characterized by corticocerebral angiomatosis, brain calcification, epilepsy, ocular alterations, mental retardation and facial nevus with color of wine port in the. The sturge weber disease is a few condition of development, not hereditary featured of harmatomatous vascular proliferation, involve the tissues of brain and face. Abstract weber s syndrome is characterized by a third nerve palsy associated with contralateral hemiparesis because of a damage to the cerebral peduncle, due to multiple etiologies. Weber, foi descrita primeiramente por schirmer 1860 e posteriormente especificada por sturge 1879 e complementada por weber 1922. A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. Parte dellencefalo che deriva dalla vescicola cerebrale media embrionale. It is characterized by a facial portwine stain, leptomeningeal angiomatosis, and glaucoma. Mesencefalo ventral, haz corticoespinal del 18 jul 2010 sindromes alternos del tallo. Weber syndrome is described often secondary to primary haemorrhages in midbrain, aneurysmal rupture, and tumours or demielinating disease. It is a dominant autosomic transmission determining multisystemic vascular dysplasia, which has been mapped to two genes, hht1 and hht2, determined by. Sturge weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in gnaq.