"Sturge-Weber Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects.
| Descriptor ID |
D013341
|
| MeSH Number(s) |
C04.557.645.375.850 C10.562.800 C14.907.077.850
|
| Concept/Terms |
Sturge-Weber Syndrome- Sturge-Weber Syndrome
- Sturge Weber Syndrome
- Syndrome, Sturge-Weber
- Parkes Weber Syndrome
- Syndrome, Parkes Weber
- Sturge Disease
- Sturge Syndrome
- Syndrome, Sturge
- Sturge's Syndrome
- Syndrome, Sturge's
- Sturge-Kalischer-Weber Syndrome
- Sturge Kalischer Weber Syndrome
- Syndrome, Sturge-Kalischer-Weber
- Sturge-Weber-Dimitri Syndrome
- Sturge Weber Dimitri Syndrome
- Syndrome, Sturge-Weber-Dimitri
- Sturge-Weber-Krabbe Syndrome
- Sturge Weber Krabbe Syndrome
- Syndrome, Sturge-Weber-Krabbe
- Angiomatosis Oculoorbital-Thalamic Syndrome
- Encephalofacial Hemangiomatosis Syndrome
- Hemangiomatosis Syndrome, Encephalofacial
- Syndrome, Encephalofacial Hemangiomatosis
- Meningo-Oculo-Facial Angiomatosis
- Angiomatosis, Meningo-Oculo-Facial
- Meningo Oculo Facial Angiomatosis
- Meningofacial Angiomatosis-Cerebral Calcification Syndrome
- Neuroretinoangiomatosis
- Parkes-Weber Syndrome
- Syndrome, Parkes-Weber
- Phakomatosis, Sturge-Weber
- Phakomatosis, Sturge Weber
- Sturge-Weber Phakomatosis
|
Below are MeSH descriptors whose meaning is more general than "Sturge-Weber Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Sturge-Weber Syndrome".
This graph shows the total number of publications written about "Sturge-Weber Syndrome" by people in this website by year, and whether "Sturge-Weber Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Sturge-Weber Syndrome" by people in Profiles.
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Limb Overgrowth with Vascular Anomalies. J Pediatr. 2022 01; 240:308-309.
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An unusual spiculated presentation of follicular porokeratosis. Dermatol Online J. 2019 Jul 15; 25(7).
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Combined surgical and endovascular treatment of complex high-flow conus medullaris arteriovenous fistula associated with Parkes Weber syndrome: case report. J Neurosurg Spine. 2016 Aug; 25(2):234-8.
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Surgical management of glaucoma with the sturge weber syndrome. Int Ophthalmol Clin. 2008; 48(2):63-78.
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The tram-track sign: cortical calcifications. Radiology. 2004 May; 231(2):515-6.
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[Genetic factors related to intracranial arteriovenous malformations]. Neurochirurgie. 2001 May; 47(2-3 Pt 2):154-7.
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Expression of basement membrane and endothelial cell adhesion molecules in vascular malformations of the brain: preliminary observations and working hypothesis. Neurol Res. 1995 Feb; 17(1):49-58.
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Isolated frontal lobe calcification in Sturge-Weber syndrome. AJNR Am J Neuroradiol. 1988 Jan-Feb; 9(1):203-4.
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Ocular manifestations of the neurocutaneous syndromes. Pediatr Dermatol. 1984 Oct; 2(2):98-117.