ENFERMEDAD STURGE WEBER PDF

El síndrome de Sturge-Weber es un trastorno vascular congénito . el 77% de los pacientes, siendo la enfermedad más frecuente el glaucoma (46%), seguido . ORPHA Synonym(s). Encephalofacial angiomatosis; Encephalotrigeminal angiomatosis; SWS; Sturge-Weber-Dimitri syndrome; Sturge-Weber-Krabbe. Meanings of “enfermedad de sturge-weber” in English Spanish Dictionary: 1 result(s) Meanings of “enfermedad de sturge-weber” with other terms in English.

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Central Nervous SystemPaediatrics. Sometimes, the PWS may also cover the maxillary and mandibular areas of the face and in some cases may extend to the trunk and limbs. Read it at Google Books – Find it at Amazon.

Case 8 Case 8. To quiz yourself on this article, log in to see multiple choice questions. Diagnosis is suspected upon clinical examination. Si continua navegando, consideramos que acepta su uso. Loading Stack – 0 images remaining. Sturge-Weber syndrome was first wbeer by Sturge infollowed by Weber and Volland in who described the intracranial calcification.

The finding usually becomes evident between 2 and 7 years of age 2.

It is characterized by a facial Port-wine stain, leptomeningeal angiomatosis, and glaucoma. Prognosis depends on the extent of leptomeningeal involvement and the severity of the glaucoma. All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style.

Subscribe to our Newsletter. For all other comments, please send your remarks via contact us. Unable to process the form. Go to enfermedsd members area of the website of the AEDV, https: Skull x-rays were historically useful and capable of identifying the gyriform calcification of the subcortical white matter although they no longer play a significant role in the diagnosis or management of this condition.

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Case 10 Case Neuroimaging studies show leptomeningeal angiomatosis, supporting diagnosis.

Case 1 Case 1. Specialised Social Services Eurordis directory.

Term Bank – enfermedad de sturge-weber – Spanish English Dictionary

Sturge-Weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in GNAQ ; it affects 1 in every 20, to 50, newborns. Check for errors and try again. Case 7 Case 7. Previous article Next article. Epidemiology Clinical presentation Pathology Radiographic features Treatment and prognosis History and etymology Differential diagnosis Related articles References Images: Cerebral vascular malformations are also present.

In the year has been indexed in the Medlinedatabase, and has become a vehicle for expressing the most current Spanish medicine and modern. Granell bE.

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SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Migraines and stroke-like episodes are also very common. Management and treatment Laser treatment, usually started in infancy, reduces the progression of the PWS and allows partial, or in rare cases, complete, clearance.

The prognosis depends on the severity enffermedad the epileptic crises which may lead to variable degrees of psychomotor regression and intellectual disability.

enfermedad de sturge-weber

Frequent ophthalmologic examinations should be carried out in cases with glaucoma. Radiographic identification of cerebral calcification was first described by Dimitri in Higueros aE. Additional information Further information on this disease Classification s 8 Gene s 1 Disability Clinical signs and symptoms Publications in PubMed Other website s Prognosis depends on the extent of leptomeningeal involvement and the severity of the glaucoma. Standard treatment for Sturge-Weber syndrome includes laser treatment for the Port-wine stain, anticonvulsants, and medical or surgical treatment for the glaucoma.

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Laser treatment, usually started in infancy, reduces the progression of the PWS and allows partial, or in rare cases, complete, clearance. Glaucoma may be present at birth or develop later. Case 12 Case The documents contained in this web site are presented for information purposes only. You can also scroll through stacks with your mouse wheel or the keyboard arrow keys.

Pemphigus Vegetans in the Inguinal Folds. Case 11 Case Read this article in English.

Síndrome de Sturge-Weber: revisión | Actas Dermo-Sifiliográficas (English Edition)

Professionals Summary information Greekpdf Polskipdf Anesthesia guidelines Englishpdf. The facial capillary malformation classically referred to as angioma is a port-wine stain PWS that is generally present at birth and located on the forehead or upper eyelid on one or both sides of the face.

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