Results 81 to 90 of about 5,272 (228)

Special consideration while planning exotropia surgery in high myopic adults

Journal of the Egyptian Ophthalmological Society
Aim To follow a new parameter in managing exotropia in high myopic adults. Patients and methods This study included 30 adult patients, having high myopia, more than −8 D in one or both eyes, and suffering from exotropia.
Karim Gaballah, Dalal Shawky
doaj   +1 more source

Absence of Syndactyly Associated With the Common Apert FGFR2 S252W Mutation: A Clinical Report and Likely Molecular Explanation

American Journal of Medical Genetics Part A, Volume 200, Issue 1, Page 215-222, January 2026.
ABSTRACT Apert syndrome is a recognizable craniofacial condition characterized by craniosynostosis, hypertelorism, exorbitism, midface hypoplasia, and complex symmetrical bony and cutaneous ‘mitten’ syndactyly of all four limbs. Around 98% of affected patients have one of two heterozygous missense variants in the FGFR2 gene, encoding either p ...
Ramy Saad, Claire Lawn, Honor Gartland, Louisa Steel, Caitlin Barns‐Jenkins, Greg James, Eleanor Hay, Andrew O. M. Wilkie, Louise C. Wilson   +8 more
wiley   +1 more source

Kinetics of Fluorescein in Tear Film After Eye Drop Instillation in Beagle Dogs: Does Size Really Matter?

Frontiers in Veterinary Science, 2019
The study aimed to determine the impact of drop size on tear film pharmacokinetics and assess important physiological parameters associated with ocular drug delivery in dogs.
Lionel Sebbag, Lionel Sebbag, Nicolette S. Kirner, Rachel A. Allbaugh, Alysha Reis, Jonathan P. Mochel   +5 more
doaj   +1 more source

Morphometric Analysis of the Palpebral Fissure and Canthal Distance in Serbian Young Adults [PDF]

, 2020
Nikola Knezi, Vladimir Isaretovic, Ivan Adjic, Nikola Babić, Dušica Marić, Ljubica Stojsic-Dzunja   +5 more
openalex   +1 more source

Add‐On Telitacicept Significantly Improves Outcome of Patients With Refractory Ocular Myasthenia Gravis a Real‐World Case Series

Brain and Behavior, Volume 16, Issue 1, January 2026.
6/7 patients achieved CMI by the third follow‐up, sustained to the fourth follow‐up, and 4/6 reached MSE by the fifth follow‐up. First real‐world evidence of adding telitacicept efficacy in refractory ocular MG symptoms Abstract Introduction Refractory ocular myasthenia gravis (MG) represents a significant therapeutic challenge, as conventional ...
Jing Lin, Yue Li, Mengcui Gui, Bitao Bu, Zhijun Li   +4 more
wiley   +1 more source

Congenital third nerve palsy with synergistic depression on attempted adduction and trigemino-oculomotor synkinesis: Underpinnings of a spectral dysinnervation disorder

Indian Journal of Ophthalmology, 2016
The authors describe a case of congenital partial pupil-sparing third cranial nerve palsy with absent adduction, synergistic depression of globe and widening of palpebral fissure on attempted adduction and synergistic elevation and adduction on mouth ...
Pramod Kumar Pandey, Vishaal Bhambhwani, P C Ranjith, Mandar Kadav, C Aparnaa   +4 more
doaj   +1 more source

Right Corneal Degeneration in Region of Palpebral Fissure, Associated with Rigidity of Eyelids [PDF]

, 1930
J. H. Doggart
openalex   +1 more source

KBG Syndrome: A Case Report and Longitudinal Assessment of Long‐Acting Recombinant Human Growth Hormone Therapy

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT This case analysis examines the clinical data, molecular genetic testing results, and 20‐month clinical data of long‐acting recombinant human growth hormone (rhGH) treatment in a child with KBG syndrome (KBGS). The child exhibited a c.1591delG frameshift mutation in the ANKRD11 gene associated with KBGS, a variant not previously reported ...
Hui Nan, Pu Zhang, Jing Qian
wiley   +1 more source

Facial Dimensions in Infants

Nigerian Journal of Paediatrics
Anthropometric measurements of facial dimensions were studied in randomly selected 290 infants. Values were obtained and reference curves for inner canthal, outer canthal, palpebral fissure lengths, and canthal indices were con- structed.
OO Omotade , CM Kayode , CM Kayode , AA Adeyemo   +3 more
doaj  

Identification of Additional Cases of Severe Neonatal GABA‐Transaminase Deficiency

JIMD Reports, Volume 67, Issue 1, January 2026.
ABSTRACT GABA‐transaminase (GABA‐T) deficiency is a rare disorder of GABA metabolism characterized by neonatal encephalopathy, epilepsy, hypotonia and intellectual disability. It is caused by biallelic pathogenic variants in the ABAT gene. We report a case of a newborn female born to a G10P5 mother, with abnormal fetal movements and polyhydramnios in ...
Deima Alammary, Tisiana Low, Ganesh Srinivasan, Marie‐Claude Dery, Mahmoud Almutadares, Samantha Marin, Mubeen F. Rafay, Katya Rozovsky, Patrick Frosk   +8 more
wiley   +1 more source