Encephalotrigeminal angiomatosis, also called Sturge-Weber syndrome (SWS), is a syndrome of etiology which is not yet clear. It is a nonhereditary condition. The clinical features include pigmentation over the facial skin known as port-wine stain, abnormalities of ocular region, and central nervous system involvement as leptomeningeal angioma. In this manuscript, we present a rare case report with an unusual combination of SWS with facial lobular capillary hemangioma.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025953 | PMC |
| http://dx.doi.org/10.4103/ijabmr.IJABMR_301_19 | DOI Listing |
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