Unilateral Lennox–Gastaut syndrome associated with Klippel–Trénaunay syndrome

B Tabarki, K Hundallah, N Biary - Neurosciences Journal, 2021 - nsj.org.sa
A 2-year-old boy with Klippel-Trénaunay syndrome, characterized by extensive port-wine
staining and left lower limb hemihypertrophy, and developmental delay, with impairments in …

[CITATION][C] Klippel-Trenaunay-Weber syndrome with partial motor seizures and hemimegalencephaly

S Ahmed, R Koul, A Wailey, D Sankhala - Neurosciences Journal, 2008 - nsj.org.sa
Klippel-Trenaunay-Weber syndrome with partial motor seizures and hemimegalencephaly
Page 1 Klippel-Trenaunay-Weber syndrome with partial motor seizures and …

Action tremor caused by olivary cavernoma in Klippel–Trénaunay syndrome mimicking asymmetric essential tremor

M Südmeyer, P Maroof, A Saleh, C Hartmann… - Journal of …, 2011 - Springer
A 52-year-old right-handed woman presented with a 24-month history of a subacute and
slowly progressive action tremor (5–6 Hz) of the upper limbs with dominance for her left side …

Spinal Neurovascular Malformations in Klippel-Trenaunay Syndrome: A Single Center Study

Z Demartini Jr, AK Maeda, GL Koppe, LAM Gatto… - …, 2021 - journals.lww.com
To the Editor: We read with great interest the article by Anthony Larson, Tristan Covington,
Katelyn Anderson, Megha Tollefson, Giuseppe Lanzino, and Waleed Brinjikji entitled “Spinal …

[HTML][HTML] Lennox-Gastaut syndrome: an overview

RS Ramanathan, T Ahluwalia… - Journal of pediatric …, 2010 - journals.lww.com
Sir, A 7-year-old boy, a known case of GTCS (generalized tonic–clonic seizures) since 8
months of age whose seizures were poorly controlled with antiepileptic medications, was …

[PDF][PDF] Repetitive cerebral bleeding in an adult with Klippel-Trenaunay syndrome

A Petzold, C Bischoff, B Conrad - Journal of neurology, 2000 - discovery.ucl.ac.uk
SIRS: Klippel–Trénaunay Syndrome (KTS) is a congenital anomaly of unknown aetiology,
characterised by vascular (98%), cutaneous (72%) and skeletal (67%) symptoms [8]. Brain …

[HTML][HTML] Chiari I malformation with Klippel-Trenaunay syndrome: case report and review of the literature

IA Snee, CA Mazzola, T Sikorskyj - Child's Nervous System, 2021 - Springer
We present a rare case of an 8-year-old male with Klippel-Trenaunay syndrome (KTS) and a
Chiari I malformation (CIM). Magnetic resonance imaging (MRI) to investigate facial …

Lennox-Gastaut syndrome with band form heterotopia: a case report

YC Chen, CS Chi, SC Mak, JC Lin - … yi xue za zhi= Chinese Medical …, 1991 - europepmc.org
A 10-year-old girl with developmental delay, mental retardation and intractable seizures is
reported. She manifested clinically as Lennox-Gastaut syndrome with unknown etiology …

Teaching NeuroImage: Nevus Flammeus, Ocular Melanosis, and Seizures in Young Adult With Sturge-Weber and Klippel-Trenaunay Overlap Syndrome

K Lavanya, R Ramesh, S Shanmugam… - …, 2023 - ingentaconnect.com
An 18-year-old man with delayed gross motor and language development and congenital
glaucoma presented with recurrent seizures since 3 months of age. The seizures were …

Klippel-Trenaunay syndrome associated with hemimegalencephaly

O Jellouli, R Dafiri - Archives de Pediatrie: Organe Officiel de la …, 2014 - europepmc.org
Klippel-Trenaunay syndrome (KTS) is a rare, complex congenital vascular malformation.
This neurocutaneous syndrome can be associated with brain malformations. We report a …