Results 41 to 50 of about 2,459,279 (115)

Natural history of cerebral visual impairment in children with cerebral palsy

Developmental Medicine &Child Neurology, Volume 67, Issue 4, Page 486-495, April 2025.
This original article is commented by Williams on pages 424–425 of this issue. Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16143 Abstract Aim To longitudinally evaluate the natural history of cerebral visual impairment (CVI) in children with cerebral palsy (CP) and identify which early visual signs or symptoms are ...
Jessica Galli, Erika Loi, Stefano Calza, Serena Micheletti, Anna Molinaro, Alessandra Franzoni, Andrea Rossi, Francesco Semeraro, Lotfi B. Merabet, Elisa Fazzi   +9 more
wiley   +1 more source

Botulinum toxin-A in acute acquired comitant esotropia during COVID pandemic in children and young adolescents. [PDF]

Indian J Ophthalmol
Purpose: To study the effectiveness of botulinum toxin A (BTX-A) in the treatment of patients with acute acquired comitant esotropia (AACE) due to excessive use of mobile and laptops in the COVID era in the pediatric population and adolescents.
Pawar N, Shyam P, Ravindran M, Allapitchai F.   +3 more
europepmc   +2 more sources

Acute‐onset sagging eye syndrome

Journal of General and Family Medicine, Volume 26, Issue 2, Page 173-174, March 2025.
A 78‐year‐old woman with untreated hypertension presented to the emergency department with a 2‐day history of binocular diplopia, initially raising suspicion of neurological pathology. However, characteristic facial findings suggested sagging eye syndrome, confirmed by orbital magnetic resonance imaging.
Yusuke Ito
wiley   +1 more source

A retrospective longitudinal study of 52 Finnish patients with X‐linked retinoschisis

Acta Ophthalmologica, Volume 103, Issue 2, Page 196-204, March 2025.
Abstract Purpose To describe clinical characteristics in Finnish patients with X‐linked retinoschisis (XLRS) longitudinally with emphasis on retinal morphology and genotype–phenotype correlations. Methods A retrospective cohort study reviewed medical records from patients with genetically confirmed XLRS from the Department of Ophthalmology, Helsinki ...
Mira A. Järvinen, Rigmor C. Baraas, Anna Majander, Michael P. Backlund, Julia Krootila, Maarjaliis Paavo, Päivi Lindahl, Kristiina Vasara, Eeva‐Marja Sankila, Tero T. Kivelä, Joni A. Turunen   +10 more
wiley   +1 more source

Effect of the prism and Maddox rod test as the surgical target for type III acute acquired comitant esotropia

Frontiers in Medicine
IntroductionThis study aims to explore more accurate and efficient examination methods to provide precise target surgical measurements for patients with type III acute acquired comitant esotropia (AACE).MethodsThe study conducted a retrospective analysis
Huihang Wang, Huihang Wang, Weidong Zheng, Weidong Zheng   +3 more
doaj   +1 more source

Isolated Abducens Nerve Palsy in an Adolescent With Confounding Multisystem Serology: A Case Report and Diagnostic Review

Case Reports in Pediatrics, Volume 2025, Issue 1, 2025.
Cranial nerve palsies in pediatric patients are rare and can be challenging to diagnose due to the broad spectrum of potential causes, including infections, inflammation, neoplasms, and idiopathic conditions. Abducens nerve palsy (ANP), though uncommon, is of particular interest due to its association with both intracranial and systemic pathologies. We
Roberto Paparella, Irene Bernabei, Fabiola Panvino, Camilla Ajassa, Lorenzo Benedetti, Lucia Leonardi, Alberto Spalice, Luigi Tarani, Nikhat Kaura   +8 more
wiley   +1 more source

Expanding the phenotype of neurofibromatosis type 1 microdeletion syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Volume 196, Issue 4, December 2024.
Abstract Neurofibromatosis type 1 (NF‐1) microdeletion syndrome accounts for 5 to 11% of individuals with NF‐1. The aim of our study was to characterize a large cohort of individuals with NF‐1 microdeletion syndrome and expand its natural history.
Jenny P. Garzon, Andrea Patete, Lindsey Aschbacher‐Smith, Dima Qu'd, Geraldine Kelly‐Mancuso, Carolyn R. Raski, Allison Goetsch Weisman, Madison Hankins, Michael Sawin, Katherine Kim, Andy Drackley, Janice Zeid, K. Nicole Weaver, Robert J. Hopkin, Howard M. Saal, Joel Charrow, Elizabeth Schorry, Robert Listernick, Brittany N. Simpson, Carlos E. Prada   +19 more
wiley   +1 more source

Vestibulo-ocular reflex evaluation of the children with acquired esotropia

, 2022
Objectives: This study aims to evaluate the effects of acquired esotropia on vestibulo-ocular reflex (VOR) gain in children using video (vHIT) and functional head impulse (fHIT) tests.
TORUN TOPÇU, MERVE, Kalciog, Mahmut Tayyar, MUTLU, AHMET, Gunes, Medine, HEPOKUR, MUSTAFA, Oguz, Halit, MUTLU, BAŞAK   +6 more
core   +1 more source

Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)

American Journal of Medical Genetics Part A, Volume 194, Issue 10, October 2024.
Abstract Myhre syndrome is an increasingly diagnosed ultrarare condition caused by recurrent germline autosomal dominant de novo variants in SMAD4. Detailed multispecialty evaluations performed at the Massachusetts General Hospital (MGH) Myhre Syndrome Clinic (2016–2023) and by collaborating specialists have facilitated deep phenotyping, genotyping and
Angela E. Lin, Eleanor R. Scimone, Robyn P. Thom, Duraisamy Balaguru, T. Bernard Kinane, Peter P. Moschovis, Michael S. Cohen, Weizhen Tan, Cole D. Hague, Katelyn Dannheim, Lynne L. Levitsky, Evelyn Lilly, Daniel V. DiGiacomo, Kara M. Masse, Sarah M. Kadzielski, Claire A. Zar‐Kessler, Leo C. Ginns, Ann M. Neumeyer, Mary K. Colvin, Jack S. Elder, Christopher P. Learn, Hongmei Mou, Kathryn M. Weagle, Karen A. Buch, William E. Butler, Kenda Alhadid, Patricia L. Musolino, Sadia Sultana, Dhrubajyoti Bandyopadhyay, Otto Rapalino, Zachary S. Peacock, Elizabeth L. Chou, Gena Heidary, Aaron T. Dorfman, Shaine A. Morris, James D. Bergin, Jonathan H. Rayment, Lisa A. Schimmenti, Mark E. Lindsay, MGH Myhre Syndrome Study Group, Luisa Paredes Acosta, Jennifer A. Bassetti, Sarah Bowdin, Joy A. Bress, Joseph A. Camarda, Joanne S. Chiu, C. Eduardo Corrales, Gregory Costain, Mary Beth P. Dinulos, Rajiv Devanagondi, Emily S. Doherty, John Dykes, Ann‐Christine Duhaime, Robert F. English, Elizabeth Fieg, Nora D. B. Friedman, Carl P. Garabedian, Samantha Glowacki, Barbara R. Gottlieb, Mary Hope Griffin, Frances J. Hayes, Stephanie R. Hicks, Alicia M. Hinze, Brigette A. Jason, Joel Krier, Kristen Lindgren, Michael Lyons, Adnan Majid, Hannah C. Mannem, Marie McDonald, Vinod Misra, Amy Morgan, Barbara J. Nath, Michele Ploutz, Eloise J. Prijoles, Margaret B. Pulsifer, Alicia M. Quesnel, Farrah Rajabi, Mersedeh Rohanizadegan, Ana Maria Rosales, Holly Rothermel, Edith Schussler, Elizabeth A. Sellars, Joseph Shieh, Stephanie Sherrill, Heidi Taska‐Tench, Matthew Thompson, George E. Tiller, Stephanie E. Vallee, David Viskochil, Stephanie Ware, Rachel C. Whooten, Samuel Yang, Elaine H. Zackai, Dala Zakaria   +94 more
wiley   +1 more source

Age‐related nonparalytic hypertropia: Clinical features

Acta Ophthalmologica, Volume 102, Issue 6, Page 683-689, September 2024.
Abstract Purpose Age‐related nonparalytic hypertropia (ARNH) is reported to be involved in sagging eye syndrome, where excyclotorsion is large and the lower eye is more extorted. The primary aim of this study was to describe the clinical profiles of patients with ARNH.
Akihiko Oohira
wiley   +1 more source