Results 61 to 70 of about 1,569,833 (157)

Head and Neck Clinical Signs Associated With Diseases: A Scoping Review

Special Care in Dentistry, Volume 46, Issue 3, May/June 2026.
ABSTRACT Objective Clinical signs observed during head and neck examination offer important diagnostic clues. This scoping review aimed to identify key clinical signs in this region associated with diseases and syndromes and to map them according to their location. Methods An electronic literature search was performed in five databases (Embase, LILACS,
Helena Miguel Cotter, Mateus José Dutra, Gustavo Davi Rabelo, Ana Carolina Prado Ribeiro, Marcio Ajudarte Lopes, Márcio Diniz‐Freitas, Luiz Paulo Kowalski, Alan Roger Santos‐Silva, Caique Mariano Pedroso   +8 more
wiley   +1 more source

Analysis of Sturge–Weber syndrome: A retrospective study of multiple associated variables

Neurología (English Edition), 2017
Introduction: Sturge–Weber syndrome is a congenital vascular disorder characterised by facial capillary malformation (port-wine stain) associated with venous and capillary malformations in the brain and eye. Neurological symptoms and alterations in other
A.I. Maraña Pérez, M.L. Ruiz-Falcó Rojas, V. Puertas Martín, J. Domínguez Carral, I. Carreras Sáez, A. Duat Rodríguez, V. Sánchez González   +6 more
doaj   +1 more source

Klippel–Trenaunay and Sturge–Weber Overlap Syndrome with KRAS and GNAQ mutations

Annals of Clinical and Translational Neurology, 2020
Patients with combined phenotypes of Sturge–Weber syndrome and Klippel–Trenaunay syndrome have been reported, though the underlying genetic spectrum in these individuals remains to be elucidated.
Ruojie He, Songjie Liao, Xiaoli Yao, Ruxun Huang, Jinsheng Zeng, Jian Zhang, Jian Yu   +6 more
doaj   +1 more source

An Infant With Phakomatosis Pigmentovascularis Complicated by Multisystem Damage: Elaborate Care Leads to a Positive Outcome

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT This report highlights the value of multidisciplinary collaboration, personalized care, dynamic monitoring of seizure activity, and innovative skin management in a 2‐month‐old with Phakomatosis Pigmentovascularis. In parallel, the nursing team implemented a multidimensional “medical–social–psychological” support model, providing psychological ...
Kaimin Chen, Xiaoxia Huang, Xin Jin, Lilan He, Mingzhu He, Wenli Shen, Yuling Zheng   +6 more
wiley   +1 more source

Population‐Based Cohort Study for Development of National Retinopathy of Prematurity Screening Criteria

Acta Paediatrica, Volume 115, Issue 3, Page 671-678, March 2026.
ABSTRACT Aim Screening criteria for retinopathy of prematurity (ROP) vary among countries. Early detection of ROP and minimising the burden of screening are important. Methods We analysed data from very preterm infants born in Switzerland between 2006 and 2022.
R. Gerull, C. Sanchez, A. Atkinson, M. Schuler‐Barazzoni, M. Adams, F. Barcos Munoz, C. Gerth‐Kahlert, S. M. Schulzke, on behalf of the Swiss Neonatal Network, Ph. Meyer, L. Eisenhut, M. Bryant, A. Kidszun, T. Riedel, M. Gebauer, B. Rogdo, B. Wagner, R. E. Pfister, J.‐F. Tolsa, J. Schneider, M. Stocker, P. Gessler, B. Laubscher, J. Llor, A. Malzacher, A. Birkenmaier, L. Hegi, V. Bernet, M. Tomaske, D. Bassler, V. Cannizzaro, C. Hagmann   +31 more
wiley   +1 more source

Unusual Cause of Facial Asymmetry: Sturge-Weber Syndrome

, 2019
Sturge-Weber syndrome is a rare neurocutaneous disease, also called encephalotrigeminal angiomatosis. In this study, we aimed to present a patient with Sturge-Weber syndrome who had atypical radiological findings and with dural arteriovenous fistula. The
Kiziloglu, Alper, Hayri Ogul, Alper Kiziloglu, OĞUL, Hayri   +3 more
core   +1 more source

The epileptologist's perspective of focal cortical dysplasia type 3: From concept to management

Epilepsia, Volume 67, Issue 3, Page 1017-1031, March 2026.
Abstract The recent International League Against Epilepsy (ILAE) official and updated classification of focal cortical dysplasia (FCD) includes a third type—FCD type 3—characterized by architectural abnormalities (cortical dyslamination) associated with another “principal” lesion: hippocampal sclerosis (HS), developmental tumors, vascular malformations,
André Palmini, Francine Oliveira, Eliseu Paglioli, Harvey Sarnat, Ricardo Paganin, Ricardo Soder, William Martins, Rafael Paglioli, Thomas Frigeri, Fernanda Schuh, Vicenzo Zarpellon   +10 more
wiley   +1 more source

Hypothyroidism and Sturge-Weber Syndrome

, 2008
Two children out of 83 (2.4%) with Sturge-Weber syndrome, who attended a multidisciplinary center at Johns Hopkins Hospital, Baltimore, MD, were found to have central ...
J Gordon Millichap
core   +1 more source

Does Early Laser Treatment of Capillary Malformations Lead to More Favorable Outcomes?

The Laryngoscope, Volume 136, Issue 7, Page 2854-2855, July 2026.
Larkin Harris, Reema Padia
wiley   +1 more source

Case Report of Rasmussen's Encephalitis With a Decade of Refractory Epilepsy and Hemispheric Atrophy

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Rasmussen's encephalitis (RE) is a rare, chronic inflammatory neurological disorder affecting one cerebral hemisphere and presenting with drug‐resistant epilepsy, progressive hemiparesis, and cognitive decline. This case report describes the clinical course and management of a 21‐year‐old patient with refractory epilepsy and progressive ...
Sajjad Al‐Badri, Aditya Duhan, Rania H. Al‐Taie, Abbas Hamza Abbas, Ayah Abdulgadir, Ibrahim Khalil, Zaryab Bacha, Noran Al‐Gizey   +7 more
wiley   +1 more source