 Sturge-Weber Syndrome
"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
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| MeSH Number(s) |
C04.557.645.375.850 C10.562.800 C14.907.077.850
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| 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
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 | | 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Sturge-Weber Syndrome" by people in Profiles.
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Bertino F, Braithwaite KA, Hawkins CM, Gill AE, Briones MA, Swerdlin R, Milla SS. Congenital Limb Overgrowth Syndromes Associated with Vascular Anomalies. Radiographics. 2019 Mar-Apr; 39(2):491-515.
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J?lich K, Neuberger I, Sahin M, Takeoka M, Pinto A, Prabhu SP. Yield of Emergent Neuroimaging in Patients With Sturge-Weber Syndrome Presenting With Acute Neurologic Symptoms. J Child Neurol. 2019 01; 34(1):17-21.
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Yukna RA, Cassingham RJ, Carr RF. Peridontal manifestations and treatment in a case of Sturge-Weber syndrome. Oral Surg Oral Med Oral Pathol. 1979 May; 47(5):408-15.
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