"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 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2019 | 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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The Pathogenesis of Port Wine Stain and Sturge Weber Syndrome: Complex Interactions between Genetic Alterations and Aberrant MAPK and PI3K Activation. Int J Mol Sci. 2019 May 07; 20(9).
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Sturge-Weber syndrome variant with atypical intracranial findings: case report. J Child Neurol. 2006 Feb; 21(2):155-7.
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Progressive venous occlusion in a neonate with Sturge-Weber syndrome: demonstration with MR venography. AJNR Am J Neuroradiol. 1995 Aug; 16(7):1539-42.