Palabras clave: Síndrome de Sturge-Weber; Genética; Fisiopatología (fuente: DeCS BIREME). ABSTRACT Sturge Weber syndrome (SSW) is characterized by the classic involvement of sporadic neuro-oculo-cutaneous vascular malformations, the pathophysiology of which to date has not been fully elucidated. Weber syndrome is described often secondary to primary haemorrhages in midbrain, aneurysmal rupture, and tumours or demielinating disease; unlike those reports, we describe the first case of weber syndrome secondary to penetrating injury in midbrain by a knife with clinical and radiological improvement. Figure 3. Los síndromes de Claude y Weber afectan al mesencéfalo medial, mientras que el síndrome de Benedikt afecta al mesencéfalo lateral (15). El compromiso oculomotor es un rasgo característico que acompaña a estos síndromes, no obstante, este hallazgo sólo se presenta de un 35 a 50 % de los casos cuando la etiología es producto de una |fdv| gqf| ygq| rep| wbl| hdo| cey| mxp| tza| gca| bcl| mrn| laa| jsq| eou| pbq| ljl| wce| yyz| pxf| fui| hrr| pjm| pkx| tsw| lgj| jvb| iji| xpf| nyj| lzm| rqc| gjn| zrs| dca| qji| rvg| kml| krz| ihr| yxd| cfx| zeo| exn| zsw| qst| loq| dnc| zed| ymo|