"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 |
|---|
| 2007 | 1 | 0 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2021 | 2 | 0 | 2 |
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Below are the most recent publications written about "Sturge-Weber Syndrome" by people in Profiles.
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Port-wine Birthmarks: Update on Diagnosis, Risk Assessment for Sturge-Weber Syndrome, and Management. Pediatr Rev. 2022 Sep 01; 43(9):507-516.
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Consensus Statement for the Management and Treatment of Sturge-Weber Syndrome: Neurology, Neuroimaging, and Ophthalmology Recommendations. Pediatr Neurol. 2021 08; 121:59-66.
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Consensus Statement for the Management and Treatment of Port-Wine Birthmarks in Sturge-Weber Syndrome. JAMA Dermatol. 2021 01 01; 157(1):98-104.
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Focal resection of leptomeningeal angioma in a rare case of Sturge-Weber syndrome without facial nevus. Pediatr Neurosurg. 2013; 49(2):99-104.
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Lymphatic abnormalities are associated with RASA1 gene mutations in mouse and man. Proc Natl Acad Sci U S A. 2013 May 21; 110(21):8621-6.
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MRI with diffusion-weighted imaging in children and young adults with simultaneous supra- and infratentorial manifestations of Sturge-Weber syndrome. J Neuroradiol. 2010 Mar; 37(1):51-9.
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Sturge-Weber syndrome with cerebellar involvement. J Neuroradiol. 2009 Mar; 36(1):57-60.
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[Sturge-Weber syndrome. Early manifestation and visualization of disease course]. Radiologe. 2007 Dec; 47(12):1126-30.
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Central nervous system perfusion and metabolism abnormalities in Sturge-Weber syndrome. J Child Neurol. 1997 Apr; 12(3):218-22.
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Epilepsy surgery in infants. Epilepsia. 1996 Jul; 37(7):625-37.