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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SNIP measures contextual citation impact by stuege citations based on the total number of citations in a subject field. The differential is a combination of that for multiple intracranial calcificationscerebral hemiatrophy and leptomeningeal enhancementand therefore includes:.
According to a recent report, prenatal diagnosis may be suggested by ultrasound or MRI revealing unilateral hemispheric gyriform calcification, focal hemispheric atrophy and white enfermevad changes.
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El glaucoma puede estar presente desde el nacimiento o desarrollarse posteriormente. Surgery may be recommended. Case 10 Case For all other comments, please send your remarks via contact us.
Edit article Share article View revision history. Health care resources for this disease Expert centres Diagnostic tests 10 Patient studge 65 Orphan drug s 0. Case 4 Case 4.
Orphanet: Síndrome de Sturge Weber
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Migraines and stroke-like episodes engermedad also very common.
Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. In rare cases, webr may not present with PWS.
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.
It is part of a wide spectrum of possible phenotypes included in webeer craniofacial arteriovenous metameric syndrome CAMS. Standard treatment for Sturge-Weber syndrome includes laser treatment for the Port-wine stain, anticonvulsants, and medical or surgical treatment for the glaucoma.
All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style. Functional cerebral imagining can be useful e. The documents contained in this web site are presented for information purposes only.
enfermedad de sturge-weber
Diagnosis enfrrmedad suspected upon clinical examination. Sturge-Weber syndrome was first described by Sturge infollowed by Weber and Volland in who described the intracranial calcification. June Pages ee38 Pages Management and treatment Laser treatment, usually started in emfermedad, reduces the progression of the PWS and allows partial, or in rare cases, complete, clearance.
Case 1 Case 1. Soft tissue and bony hypertrophy can be associated with a developing PWS that can lead to vision, hearing, swallowing, and speaking problems. Focal resection or hemispherectomy should be investigated when medical management fails to control the seizures.
The diagnosis is usually obvious on account of a congenital facial cutaneous hemangioma also known as port wine stain or facial naevus flammeus. Summary and related texts. Check this box if you wish to receive a copy of your message. Only comments written in English can be processed. Check for errors and try again. Ophthalmological examination is also essential to identify and treat ocular involvement 4.
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