Treatment of severe neuropatic pain for patients with the syndrome of Klippel-Trenaunay-Weber: case report

Autor: Danielle Cristina De Oliveira Soares, José Nilson Fortaleza De Araújo, Fernando Santiago Limaverde, Leila Yasmin Maria Cidrão Fortaleza, Grêta Palácio Paulino, Lean De Sousa Oliveira

Publikováno v: Journal of Health & Biological Sciences, Vol 4, Iss 4, Pp 271-274 (2016)
Journal of Health & Biological Sciences; v. 4, n. 4 (2016): Journal of Health and Biological Sciences; 271-274
Journal of Health and Biological Sciences; v. 4, n. 4 (2016): Journal of Health and Biological Sciences; 271-274
Journal of Health & Biological Sciences
Centro Universitário Christus (Unichristus)
instacron:CHRISTUS

Introduction : Klippel-Trenaunay-Weber syndrome is a rare congenital anomaly whose etiology has not yet been elucidated. It is characterized by the triad of vascular malformations, cutaneous hemangiomas and overgrowth of bone and soft tissue adjacent

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab562f786d9e64dcd796523f486d004a
http://periodicos.unichristus.edu.br/index.php/jhbs/article/view/654