| Literature DB >> 19296147 |
Maria Giuseppina Onesti1, Paolo Fioramonti, Sara Carella, Graziano Spinelli, Nicolò Scuderi.
Abstract
Sturge-Weber syndrome (also called encephalofacial or encephalotrigeminal angiomatosis) is a rare neurocutaneous syndrome characterized by facial port-wine stains in the trigeminal nerve distribution area. An innovative treatment based on surgical and laser techniques of a patient affected with Sturge-Weber syndrome is reported. The aesthetic and functional results were satisfactory.Entities:
Mesh：
Year: 2009 PMID： 19296147 DOI： 10.1007/s00266-009-9327-y
Source DB: PubMed Journal: Aesthetic Plast Surg ISSN： 0364-216X Impact factor: 2.326