| Literature DB >> 2942585 |
S Wilson, J M Venzel, R Miller.
Abstract
This syndrome, also known as encephalotrigeminal angiomatosis, is a condition with multiple clinical findings, including vascular anomalies and intraoral involvement. The patient was a nine-year-old black boy with Sturge-Weber syndrome. He had a lesion removed and diagnosed as pyogenic granuloma. There were no complications and the tissue healed normally.Entities:
Mesh:
Year: 1986 PMID: 2942585
Source DB: PubMed Journal: ASDC J Dent Child ISSN: 1945-1954