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. Sturgeweber syndrome sws, also called encephalotrigeminal angiomatosis, is a neurocutaneous disorder with angiomas that involve the. Kts is the prototype of complex overgrowth disorder associated with vascular anomalies and is the. The main etiologic factors for both ssj and ten are sulphonamides and. Stevensjohnson syndrome sjs and toxic epidermal necrolysis ten are rare lifethreatening conditions almost exclusively attributed to drugs. Klippeltrenaunay weber syndrome klippeltrenaunay disease disease, klippeltrenaunay klippel trenaunay disease klippel trenaunay weber syndrome syndrome, klippeltrenaunay weber. Dec 04, 2016 videos sobre tratamentos naturais, doencas, emagrecimento, fitness, vida saudavel e bem estar.
Encephalotrigeminal angiomatosis or sturgeweber syndrome. See actions taken by the people who manage and post content. Sturge weber syndrome is a rare congenital disorder. Sturge weber syndrome neuroretinoangiomatosis phakomatosis, sturge weber angiomatosis oculoorbitalthalamic syndrome.
The incidence in children is lower than in adults and has a better outcome. Caracterizase por uma angiomatose corticocerebral, calcificacoes cerebrais, epilepsia, afeccoes oculares, retardo mental e nevo facial. Seizures may worsen any associated cortical hypo perfusion with the potential to further impair both neurological and developmental delay. Sturgeweber syndrome, sometimes referred to as encephalotrigeminal angiomatosis, is a. Mycosplama pneumoniae infection may be involved in some cases of paediatric sjs.
Weber christian disease that was undiagnosed for 20 years and, when it was done it was possible to remission of the disease. Facebook is showing information to help you better understand the purpose of a page. Weaver syndrome is a rare autosomal dominant genetic disorder associated with rapid growth beginning in the prenatal period and continuing through the toddler and youth years. Seizures, strokelike episodes, glaucoma, headache, and developmental delay are frequently associated features. Serao comentadas caracteristicas clinicas, anatomopatologicas e diagnostico diferencial. Clinical practice guidelines for klippeltrenaunay syndrome kts.