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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The finding usually becomes evident between 2 and 7 years of age 2. Read this article in Stuge. Case 11 Case It is characterized by a facial Port-wine stain, leptomeningeal angiomatosis, and glaucoma. The leptomeningeal hemangioma results in a vascular steal affecting the subjacent cortex and white matter producing localised ischemia.

Standard treatment for Sturge-Weber syndrome includes laser treatment for the Port-wine stain, anticonvulsants, and medical or surgical treatment for the glaucoma.

To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Glaucoma may enfermedac present at birth or develop later. To quiz yourself on this article, log in to see multiple choice questions.

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

Detailed information Article for general public Svenska Radiographic identification of cerebral calcification was first described by Dimitri in Less common aspects include an increased risk of growth hormone deficiency. Antenatal diagnosis According to a recent report, prenatal diagnosis may be suggested by ultrasound or MRI revealing unilateral hemispheric gyriform calcification, focal hemispheric atrophy and white enfermddad changes.

SRJ is a prestige metric based on the idea that not all citations are the same. From Monday to Friday from 9 a. Additional information Further information on this disease Classification s 8 Gene s 1 Disability Clinical signs and symptoms Publications in PubMed Other website s SNIP measures contextual citation impact by wighting citations based on the stuege number of citations in a subject field.


You can also scroll through stacks with your mouse wheel or the keyboard arrow keys. Ophthalmological examination is also essential to identify and treat ocular involvement 4.

Sturge-Weber syndrome | Radiology Reference Article |

For all other comments, please send webef remarks via contact us. With the progression of the disease, and depending on the severity of seizures, patients may develop hemiparesis, hemiplegia, and variable degrees of intellectual disability.

Read it at Google Books – Find it at Amazon. Case 6 Case 6. Sturge-Weber syndrome is a rare syndrome, with an incidence estimated at 1 case in 20, persons Prognosis depends on the extent of leptomeningeal involvement and the severity of the glaucoma.

Eye involvement can occur at anytime but is generally observed during infancy and young adulthood. Other search option s Alphabetical list. Professionals Summary information Greekpdf Polskipdf Websr guidelines Englishpdf. If you are a member of the AEDV: Case 5 Case 5. Neuroimaging studies show leptomeningeal angiomatosis, supporting diagnosis. Frequent ophthalmologic examinations should be carried out in cases with glaucoma.

The facial capillary malformation classically referred to as angioma is a port-wine stain PWS that sture generally present at birth and located on the forehead or upper eyelid on one or both sides of the face. Migraines and stroke-like episodes are also very common. Case 13 Case Diagnostic methods Diagnosis is suspected upon clinical examination.

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

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enfermedad de sturge-weber

El glaucoma puede estar presente desde el nacimiento o desarrollarse posteriormente. Go to the members area of the website of the AEDV, https: Unable to process the enfermddad. Clinical description 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.

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. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Previous article Next article. Case 12 Case Diagnosis is suspected upon clinical examination.

Infants typically present in the first year of life with leptomeningeal angiomatosis, responsible for the occurrence of focal or complex partial seizures, early-handedness, and visual gaze preference. Therapy with eye drops is used to decrease pressure in the eye. It is part of a wide spectrum of possible phenotypes included in the craniofacial arteriovenous metameric syndrome CAMS.

Epidemiology Clinical presentation Pathology Radiographic features Treatment and prognosis History and etymology Differential diagnosis Related articles References Images: Prognosis depends on the extent of leptomeningeal involvement and the severity of the glaucoma.

Treatment revolves primarily around seizure control, with surgical resection only indicated rarely in refractory cases.