Klippel-Trenaunay syndrome and chiari I malformation. A case report and systematic review of the literature

Autor: D. Giakoumettis, T. Vogiatzoglou, G. Vavoulis, B. Almasarwah, K. Tilidou, A. Tsitlakidis, K. Vlachos

Publikováno v: Brain and Spine, Vol 4, Iss , Pp 104149- (2024)

Introduction: Klippel-Trenaunay Syndrome (KTS) is a rare congenital condition characterized by vascular malformations, bone abnormalities, and limb overgrowth. The genetic basis of KTS is not fully understood, and the diagnosis relies on clinical fea

Externí odkaz: https://doaj.org/article/7c144f7133bc427a98c125113420b8a7

An Update on Spinal Dural Arteriovenous Fistulae: Case Series and Systematic Review.

Autor: Vavoulis G Jr; Neurosurgery, KAT Attica General Hospital, Athens, GRC., Giakoumettis D; Neurosurgery, Agios Savvas Attica General Hospital, Athens, GRC., Tsitlakidis A; Neurosurgery, KAT Attica General Hospital, Athens, GRC., Karagianni A; Neurosurgery, KAT Attica General Hospital, Athens, GRC., Almasarwah B; Neurosurgery, KAT Attica General Hospital, Athens, GRC., Vogiatzoglou T; Neurological Surgery, KAT Attica General Hospital, Athens, GRC., Amanatidou E; Neurosurgery, KAT Attica General Hospital, Athens, GRC., Rados K; Neurosurgery, KAT Attica General Hospital, Athens, GRC., Vlachos K; Neurosurgery, KAT Attica General Hospital, Athens, GRC.

Publikováno v: Cureus [Cureus] 2024 Jul 27; Vol. 16 (7), pp. e65537. Date of Electronic Publication: 2024 Jul 27 (Print Publication: 2024).