Results 11 to 20 of about 1,487,242 (142)

Marcus Gunn jaw-winking syndrome: A case report

Acta Marisiensis - Seria Medica, 2023
Marcus Gunn jaw wink phenomenon or Trigeminal oculomotor synkinesis, is a congenital disorder in which the upper lid moves synkinetically in response to jaw movement during chewing. The term synkinesis describes the simultaneous movement or a coordinated
Sathish Sivan, Subramani Manonmani, Patel Pranay, Hirani Nidhi, Arjunan Priyadharshini   +4 more
doaj   +2 more sources

Síndrome de Marcus Gunn. Presentación de un caso Marcus Gunn syndrome. A case report

Revista de Ciencias Médicas de Pinar del Río, 2011
El fenómeno de Marcus Gunn es un movimiento congénito asociado trigémino oculomotor que afecta a los músculos elevadores del párpado y los de la masticación.
Sahely Sixto Fuentes, Annia Dolores Gorte Quiñones, Kenia Ramos Padilla, Humberto Valdés Hernández, Razel Martínez Quetglas   +4 more
doaj   +1 more source

A 7-year old female with arthrogryposis multiplex congenita, Duane retraction syndrome, and Marcus Gunn phenomenon due to a ZC4H2 gene mutation: a clinical presentation of the Wieacker-Wolff syndrome. [PDF]

Ophthalmic Genet, 2021
Godfrey D, Torres A, Heidary G, Zahoor H, Lee A, Berry G, Engle E.   +6 more
europepmc   +2 more sources

FREQUENCY AND ASSOCIATIONS OF MARCUS GUNN PHENOMENON IN CONGENITAL PTOSIS [PDF]

, 2021
Objective: To determine the frequency and various associations of Marcus Gunn Phenomenon in patients of congenital ptosis. Study Design: Cross-sectional observational study.
Maqsood Ahmad, Usama Iqbal, Hafiza Sadia Imtiaz, Ibrar Hussain, Syed Imad Zahir, Muhammad Sharjeel   +5 more
core   +1 more source

Olfactory Dysfunction in Children: A Scoping Review

Otolaryngology–Head and Neck Surgery, Volume 169, Issue 6, Page 1399-1408, December 2023., 2023
Abstract Objective Olfactory disorders are well‐studied in the adult population, however, there is a paucity of literature characterizing olfactory dysfunction in pediatric patients. The purpose of this scoping review was to identify known causes of olfactory loss in pediatric populations, clarify the extent of use and validity of smell tests, and ...
Jennifer Eva Payandeh, Mehras Motamed, Keshinisuthan Kirubalingam, Neil K. Chadha   +3 more
wiley   +1 more source

Randomised, placebo‐controlled trial and meta‐analysis show benefit of ondansetron for irritable bowel syndrome with diarrhoea: The TRITON trial

Alimentary Pharmacology &Therapeutics, Volume 57, Issue 11, Page 1258-1271, June 2023., 2023
Summary Background Ondansetron may be beneficial in irritable bowel syndrome with diarrhoea (IBS‐D). Aim To conduct a 12‐week parallel group, randomised, double‐blind, placebo‐controlled trial of ondansetron 4 mg o.d. (titrated up to 8 mg t.d.s.) in 400 IBS‐D patients.
David Gunn, Rabia Topan, Lorna Barnard, Ron Fried, Ivana Holloway, Richard Brindle, Maura Corsetti, Mark Scott, Adam Farmer, Kapil Kapur, David Sanders, Maria Eugenicos, Nigel Trudgill, Peter Whorwell, John Mclaughlin, Ayesha Akbar, Lesley Houghton, Phil G. Dinning, Qasim Aziz, Alexander C. Ford, Amanda J. Farrin, Robin Spiller   +21 more
wiley   +1 more source

Novel noncanonical splice site variant causes mild CHD7‐related disorder with variable intrafamilial expressivity

American Journal of Medical Genetics Part A, Volume 191, Issue 4, Page 1128-1132, April 2023., 2023
Abstract The clinical diagnosis criteria for CHARGE syndrome have been revised several times in the last 25 years. Variable expressivity and reduced penetrance are known, particularly in mild and familial cases. Therefore, it has been proposed to include the detection of a pathogenic CHD7 variant as a major diagnostic criterion.
Felix Boschann, Sabine Kosmehl, Marc Bloching, Johannes Grünhagen, Gabriele Hildebrand, Denise Horn, Stefan Lyutenski   +6 more
wiley   +1 more source

Laser‐Assisted In Situ Keratomileusis Surgery on a Patient with Myelin Oligodendrocyte Glycoprotein Antibody‐Associated Disease or Neuromyelitis Optica Spectrum Disorder

Case Reports in Ophthalmological Medicine, Volume 2023, Issue 1, 2023., 2023
Myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) and neuromyelitis optica spectrum disorder (NMOSD) are rare central demyelinating diseases that may affect refractive surgery outcomes. Optic neuritis and brainstem syndromes affecting cranial nerves are particularly relevant to corneal refractive surgery (CRS), such as laser ...
Majid Moshirfar, Duncan J. Williams, Melody Ziari, Meagan D. Seay, Yasmyne C. Ronquillo, Stephen G. Schwartz   +5 more
wiley   +1 more source

Clinical and imaging clues to the diagnosis and follow‐up of ptosis and ophthalmoparesis

Journal of Cachexia, Sarcopenia and Muscle, Volume 13, Issue 6, Page 2820-2834, December 2022., 2022
Abstract Ophthalmoparesis and ptosis can be caused by a wide range of rare or more prevalent diseases, several of which can be successfully treated. In this review, we provide clues to aid in the diagnosis of these diseases, based on the clinical symptoms, the involvement pattern and imaging features of extra‐ocular muscles (EOM).
Kevin R. Keene, Hermien E. Kan, Stijn van der Meeren, Berit M. Verbist, Martijn R. Tannemaat, Jan‐Willem M. Beenakker, Jan J.G.M. Verschuuren   +6 more
wiley   +1 more source

Is Marcus Gunn jaw winking a primitive reflex? Rat neuroanatomy [PDF]

International Journal of Ophthalmology, 2018
AIM: To investigate a possible trigeminal proprioceptive-oculomotor neural pathway and explore possible synaptic connections between neurons in this pathway. Attempt to bring a new insight to mechanism of Marcus Gunn syndrome (MGS). METHODS: Anterograde
Hou-Cheng Liang, Jing-Dong Zhang, Pi-Fu Luo, Ying Qiao, An-Le Su, Ting Zhang, Hong-Na Zhu   +6 more
doaj   +1 more source