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Diagnostic dilemma: Sturge-Weber syndrome, without facial nevus
Sturge-Weber syndrome (SWS), a rare sporadic neurocutaneous disease, is characterized by a congenital unilateral port-wine nevus affecting the area innervated by V1, ipsilateral leptomeningeal angiomatosis, and calcification in the occipital or frontoparietal region and glaucoma/vascular eye abnorma...
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| Yayımlandı: | J Neurosci Rural Pract |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications & Media Pvt Ltd
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4244768/ https://ncbi.nlm.nih.gov/pubmed/25552865 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-3147.143215 |
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