Sturgeweber syndrome sws is a rare neurocutaneous syndrome that is manifested by overt neurological and covert psychiatric features. Seizures in sws usually start as partial or focal seizures that can spread to a generalized seizure. Sturge weber syndrome with epilepsy and bilateral intracranial calcifications at the neonatal period. Sturgeweber syndrome, include septal defects, valvular anomlies, transposition of the great vessels, aortic coarctation and rarely deep arteriovenous malformations.
Serao comentadas caracteristicas clinicas, anatomopatologicas e diagnostico diferencial. When you add multiple files together, you maintain the size and orientation of all the pages within the original files. When omd is combined with blepharospasm, it may be referred to as meiges syndrome named after henri meige, the french neurologist who first described the symptoms in detail in 1910. It is caused by midbrain infarction as a result of occlusion of the paramedian branches of the posterior cerebral artery or of basilar bifurcation perforating arteries. Webers syndrome, also known as superior alternating hemiplegia, is a form of stroke characterized by the presence of an ipsilateral oculomotor nerve palsy and contralateral hemiparesis or hemiplegia. Seizures may worsen any associated cortical hypo perfusion with the potential to further impair both neurological and developmental delay. Sturgeweber syndrome in a 14yearold girl without facial naevus. Pdf sturgeweber syndrome sws is a sporadic, congenital disorder that impairs the.
It is actually a combination of two forms of dystonia, blepharospasm and oromandibular dystonia omd. Sturgeweber syndrome sws is a neurocutaneous disorder. Sturge weber syndrome encephalotrigeminal angiomatosis. Lubatkin, m, schweiger, d, weber, y 1999 top management. Non e correlata alla sindrome di sturgeweber o alla sindrome di klippeltrenaunay. Hr practices during postmerger conflict and merger performance. Esta facomatose, tambem conhecida como angiomatose encefalotrigeminal, e definida pela triade classica. To discuss the management and treatment and prognosis of. Sturge weber syndrome, include septal defects, valvular anomlies, transposition of the great vessels, aortic coarctation and rarely deep arteriovenous malformations. Keywords crosscultural conflict, hr practices, postmerger integration. Pdf merge combinejoin pdf files online for free soda pdf. Sturgeweber syndrome neuroretinoangiomatosis phakomatosis, sturgeweber angiomatosis oculoorbitalthalamic syndrome.
In 1992, weber complemented it through the documentation of these patients. Caracterizase por uma angiomatose corticocerebral, calcificacoes cerebrais, epilepsia, afeccoes oculares, retardo mental e nevo facial. The klippeltrenaunayweber syndrome 149000 is sometimes associated with sws see bonse, 1951 and nonnenmacher, 1955. The system converts your article files to a single pdf file used in. It is also known as brueghels syndrome and oral facial dystonia. To discuss the management and treatment and prognosis of patients diagnosed with the sturge weber syndrome. Weber christian disease that was undiagnosed for 20 years and, when it was done it was possible to remission of the disease. Pdf sturge weber syndrome, also known as encephalo trigeminal hemangiomatosis, is an uncommon. This is a pdf file of an unedited manuscript that has been accepted for publication. A multidisciplinary consensus for clinical care and research. Debicka and adamczak 1979 described sturgeweber syndrome in father and son, both of whom had, in addition to trigeminal angiomatous nevi, evidence of central nervous system involvement. General objective general objective specific objectives specific objectives to recognize symptoms of sturge weber syndrome. Sturge weber syndrome discussion the sturgeweber syndrome was initially described by schirmer, in 1860, and was later specified by sturge 1878, who associated the dermatological and ophthalmic changes to the diseases neurological manifestations.
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