Results 11 to 20 of about 445 (162)

Resolution of adult-onset cyclic esotropia

Journal of Clinical Ophthalmology and Research
Cyclic esotropia is a rare type of strabismus that has alternating periods of esotropia and orthotropia. We present the case of a 60-year-old male who complained of inward deviation of the right eye for 8–9 years with alternating periods of 12-h ...
Chasin Riamuk Roomching, Swatishree Nayak   +1 more
doaj   +2 more sources

Cyclic Esotropia: Surgical Treatment Results of Two Cases

Türk Oftalmoloji Dergisi, 2014
Cyclic esotropia is a rare form of strabismus characterized by alternating periods of esotropia and orthophoric (or almost orthophoric) eye position. Herein, we discuss two children with cyclic esotropia and their surgical treatment results.
Serpil Akar, Birsen Gökyiğit, Çiğdem Altan, Pelin Kaynak, Ahmet Demirok   +4 more
doaj   +2 more sources

Surgical Treatment of Sensory Cyclic Esotropia. [PDF]

Korean J Ophthalmol, 2019
Yoon JS, Kim US.
europepmc   +3 more sources

Vision Correction and Eye Surgery [PDF]

, 2022
This book focuses on the current approaches in the medical and surgical treatment of the most diffuse and important ocular diseases. It reports the latest developments in surgery (anterior segment surgery, posterior pole surgery, etc.) for various types ...

core   +1 more source

Management of Abnormal Visual Developments [PDF]

, 2021
When human beings recognize the external world, more than 80% of the information come from visual function and visual system. Normal visual development and normal binocularity are the fundamental of good visual acuity and visual functions.
Chen, Changxu, Chen, Pengfan, Chen, Xia, Chen, Xiaohang, Huang, Gantian, Liu, Longqian, Liu, Tong, Wang, Jianglan, Wang, Xi, Wu, Yifan, Zhang, Wenqiu, Zheng, Jing, Zhu, Bixia   +12 more
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A deep phenotyping experience: up to date in management and diagnosis of Malan syndrome in a single center surveillance report [PDF]

, 2022
Background Malan syndrome (MALNS) is a recently described ultrarare syndrome lacking guidelines for diagnosis, management and monitoring of evolutive complications. Less than 90 patients are reported in the literature and limited clinical information are
Accadia, Maria, Alfieri, Paolo, Bartuli, Andrea, Caciolo, Cristina, Chinali, Marcello, Cortellessa, Fabiana, Gonfiantini, Michaela V, Macchiaiolo, Marina, Mammì, Corrado, Panfili, Filippo M, Priolo, Manuela, Seri, Marco, Tartaglia, Marco, Vecchio, Davide, Zollino, Marcella   +14 more
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Genetic Diagnosis of Oculocutaneous Albinism Type 1A: A Novel <i>TYR</i> Variant. [PDF]

Clin Case Rep
ABSTRACT Oculocutaneous albinism type IA (OCA1A) is a rare autosomal recessive disorder caused by variants in the TYR gene, resulting in complete loss of tyrosinase activity and absence of melanin production. In this study, we report a novel missense variant, TYR (NM_000372.5):c.143A>C (p.Gln48Pro), found within exon 1 and mapped to chr11: g.89178096A ...
Shihab RN, Hamid RT, Neissi M, Mohammadi-Asl J, Sheikh-Hosseini M, Nekouei E.   +5 more
europepmc   +2 more sources

NEXMIF Pathogenic Variants in Individuals of Korean, Vietnamese, and Mexican Descent [PDF]

, 2022
NEXMIF pathogenic variants have been known to produce a wide spectrum of X-linked intellectual disability (ID) in both males and females. Thus far, few individuals from diverse populations have been described with NEXMIF-related disorders.
Farach, Laura S, Koenig, Mary K, Langley, Elizabeth, Mowrey, Kate, Northrup, Hope, Rodriguez-Buritica, David F   +5 more
core   +2 more sources

Supranuclear eye movements and nystagmus in children: A review of the literature and guide to clinical examination, interpretation of findings and age-appropriate norms. [PDF]

, 2018
Abnormal eye movements in children present a significant challenge to Ophthalmologists and other healthcare professionals. Similarly, examination of supra-nuclear eye movements in children and interpretation of any resulting clinical signs can seem very ...
A Bronstein, A Ghosh, AM Bronstein, C Day, C Valmaggia, C. M. Harris, CE Davies, D Mittelman, D. Osborne, E Gilad, F Blaes, F. Shawkat, FS Shawkat, FS Shawkat, G Walls, H Tsuda, H. Lee, HC Leung, HM Kang, I Casteels, I Russell-Eggitt, J Bielecki, J Wylie, J. E. Self, JB Lavrich, JW White, K Konrádsson, L Cassidy, L Cordero, M. Hedley-Lewis, M. Ranger, M. Theodorou, ML McGregor, R Fekete, R. John Leigh, RJ Admiraal, SL Bakker, W Zentmayer   +37 more
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MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome). [PDF]

, 2019
BACKGROUND: Putative nucleotidyltransferase MAB21L1 is a member of an evolutionarily well-conserved family of the male abnormal 21 (MAB21)-like proteins.
Altunoglu, U, Bakey, Z, Bauer, P, Boustany, R-M, Ercan-Sencicek, G, Gleeson, JG, Gunel, M, Hauser, N, James, KN, Kayserili, H, Maroofian, R, Miller, R, Najafi, M, Rad, A, Saeidi, K, Sahebzamani, A, Schmidts, M, Stanley, V, Wu, K, Yeşil, G, Çağlayan, AO   +20 more
core   +3 more sources