Federal University of Espirito Santo (UFES),
Espirito Santo, Vitoria/ES
Brazil
Case Report
Sturge Weber Syndrome, Klippel Trenaunay or Port Wine Stain? The Challenge of Diagnosis
Author(s): Helena Lucia Barroso dos ReisHelena Lucia Barroso dos Reis
Background: Sturge-Weber and Klippel-Trenaunay are congenital disorders characterized by the presence of vascular malformation that may indicate an incomplete mild clinical presentation and even combined together. Thus, the challenge of diagnosis and the appropriate follow-up of these patients become necessary due to the possible late onset of other alterations that are characteristic in these syndromes in order to provide a better quality of life for these patients. The aim of this study was to perform a review of literature on Sturge-Weber and Klippel-Trenaunay syndromes and to describe the report of a clinical case. Case report: A 5-year- old girl that was examined at a Stomatology Department in a Public University Hospital in the city of Rio de Janeiro – Brazil, who presented signs of one of the Sturge-Weber and Klippel-Trenaunay syndromes. She reported spontaneous na.. Read More»
DOI:
10.4172/2165-7920.1000452
Journal of Clinical Case Reports received 1345 citations as per Google Scholar report