Results 81 to 90 of about 619,894 (222)

Case series of Ectopia Lentis associated with Marfan's syndrome

Delhi Journal of Ophthalmology, 2021
Purpose: To report 4 cases of Marfan's syndrome with ectopia lentis. Methods: Case 1- Fifty year old woman presented with sudden painless diminution of vision both eye since 1 day with history of blunt trauma by wood-log.
Sagarika Laad, Harpal Singh, Satendra Singh, Parag Ramnani, Shashank Gupta, Ritu Gupta   +5 more
doaj   +1 more source

Investigation of ocular surface parameters in dogs with different cephalic conformations using veterinary ocular surface analyzer (OSA‐VET)

Veterinary Ophthalmology, Volume 28, Issue 3, Page 605-618, May 2025.
Abstract Objective To compare ocular surface parameters in dogs with different cephalic conformations and evaluate correlations among tests. Animals Studied Sixty‐eight privately owned dogs. Procedures The study categorized canine eyes into three groups based on the craniofacial ratio (CFR): brachycephaly (≤0.52), mesocephaly (>0.52 to <0.67), and ...
Yan‐Hui Li, Bianca Martins, Chung‐Tien Lin   +2 more
wiley   +1 more source

Severely subluxated crystalline lens

Journal of Cataract & Refractive Surgery Online Case Reports
A 52-year-old man presented with left eye blurring of vision for 4 days. He had undergone right phacoemulsification with capsular tension ring (CTR) and an extended depth-of-focus (EDOF) intraocular lens (IOL) 7 years prior. He denied trauma. The uncorrected vision in the right eye was 20/20, N5 for near, and left 20/60, N26 for near.
Soon-Phaik Chee, Samuel Masket, Priya Narang, David Lockington, Ahmed Assaf, Sergio Canabrava   +5 more
openaire   +1 more source

Hereditary Vitreoretinopathies: Molecular Diagnosis, Clinical Presentation and Management

Clinical &Experimental Ophthalmology, Volume 53, Issue 3, Page 281-291, April 2025.
ABSTRACT Hereditary vitreoretinopathies (HVRs), also known as hereditary vitreoretinal degenerations comprise a heterogeneous group of inherited disorders of the retina and vitreous, collectively and variably characterised by vitreal abnormalities, such as fibrillary condensations, liquefaction or membranes, as well as peripheral retinal abnormalities,
Hashem H. Ghoraba, Jonathan Sears, Elias I. Traboulsi   +2 more
wiley   +1 more source

Clinical, biochemical and molecular characteristics of classic homocystinuria in Saudi Arabia and the impact of newborn screening on prevention of the complications: A tertiary center experience

JIMD Reports, Volume 66, Issue 1, January 2025.
Abstract Background Classic homocystinuria (HCU) is a rare inborn metabolic disease that is generally asymptomatic at birth. If untreated, it can cause a wide range of complications including intellectual disability, lens dislocation, and thromboembolism.
Ahmed Sarar Mohamed, Talal AlAnzi, Amal Alhashem, Hadeel Alrukban, Fahad Al Harbi, Sarar Mohamed   +5 more
wiley   +1 more source

Genotypic Spectrum in a Cohort of Sri Lankan Patients With Homocystinuria

JIMD Reports, Volume 66, Issue 1, January 2025.
ABSTRACT Homocystinuria due to cystathionine beta‐synthase (CBS) deficiency is a rare metabolic disorder inherited as an autosomal recessive trait. Spectrum of genetic variants in CBS gene and their correlation with the phenotypes of homocystinuria in Sri Lankan patients have not been reported to date.
Hewa Warawitage Dilanthi, Kandana Liyanage Subhashinie Jayasena, Nambage Dona Priyani Dhammika, Neluwa Liyanage Ruwan Indika, Matara Mahavidanage Nishani De Silva, Imalke Kankananarachchi, Pushpa Malkanthi Gardiye Punchihewa, Dharma Irugalbandara, Sabine Schroeder, Kosala Karunaratne, Eresha Jasinge   +10 more
wiley   +1 more source

The Reclassification of a FBN1 Variant of Unknown Significance Associated With Marfan Syndrome Through Careful Clinical Correlation and Family‐Based Evaluation

Case Reports in Medicine, Volume 2025, Issue 1, 2025.
Background:Fibrillin‐1 (FBN1) is a major structural component of the extracellular matrix, providing strength and stability to tissues. Pathogenic variants lead to the development of FBN1‐associated syndromes which comprise a broad host of phenotypes, and more commonly, Marfan syndrome (MFS).
Dominique Bouhamdani, Véronique Allain, Nadia Bouhamdani, Mouna Ben Amor, Poulami Jha   +4 more
wiley   +1 more source

Clinical spectrum of bilateral microspherophakia and risk factors associated with poor visual outcomes following lensectomy surgery - A multicentric study

Indian Journal of Ophthalmology
Purpose: To study the clinical profile of patients with microspherophakia and the factors associated with poor vision following lensectomy surgery. Methods: A multicenter, retrospective, cross-sectional analysis was conducted from January 2010 to June ...
Monalisa Mohapatra, Shailja Tibrewal, Samrat Chatterjee, Pradeep Agarwal, Chintan Shah, Rajat Kapoor, Anupam Sahoo, Pradhanya Sen, Veenu Maan, Sonu Arjun Shetty, Samir Sutar, Priya Goyal, Suma Ganesh   +12 more
doaj   +1 more source

The use of iris claw intraocular lens in aphakic eyes with inadequate capsular support and in phakic eyes for correction of high refractive errors

Delta Journal of Ophthalmology, 2020
Background Iris-claw intraocular lens (IOL) implantation is effective for correction of aphakia in the absence of capsular support. Iris claw phakic IOLs lack potential size-related complications that may occur with other phakic IOLs.
Abdel-Khalik I El-Saadany, Hany A Khairy, Ghada Z Rajab, Ahmed M.S Fayed   +3 more
doaj   +1 more source

Persistent Hypotony Following Antiglaucoma Surgery: A Case Report

Case Reports in Ophthalmological Medicine, Volume 2025, Issue 1, 2025.
Background: Persistent hypotony is a rare but serious complication following antiglaucoma surgery. Identifying the cause and appropriate management is critical to prevent vision loss. Case Presentation: A 56‐year‐old male presented with 6 months of progressive vision loss in the left eye, 20 years post‐antiglaucoma surgery.
Shuxin Cai, Haibo Li, Shuimiao Chen, Ranqing Lin, Hannah Wesley   +4 more
wiley   +1 more source