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Artikel Jurnal
Anterior Chamber Migration of Dexamethasone Implant in a Patient Implanted with Carlevale Sutureless Scleral Fixation Intraocular Lens: A Case Report
Introduction: To report a case of anterior chamber migration of the dexamethasone intravitreal implant (DEX-I) through a new type of scleral fixated lens, the Carlevale® intraocular lens (IOL) (Cutting Edge, Italy). Case Presentation: A 74-year-old pseudophakic man with a history of macular edema…
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Artikel Jurnal
A 27-Gauge Light Pipe-Assisted Modified Kebab Technique for Safe Retrieval of a Dropped Lens Nucleus: A Case Report
Introduction: Management of dropped lens nuclei can be challenging, and several approaches have been reported, including perfluorocarbon liquid (PFCL) flotation and the kebab technique with intraocular diathermy. However, these approaches require dedicated instruments and may involve risks such as…
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Artikel Jurnal
Treat-and-Extend Faricimab for Macular Neovascularization in Angioid Streaks: A Report of Two Cases
Introduction: Angioid streaks (AS) are a rare retinal disorder that leads to progressive vision loss, particularly when complicated by macular neovascularization (MNV). Anti-vascular endothelial growth factor agents are the first-line treatment for MNV with AS; however, the optimal treatment…
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Artikel Jurnal
Probable Arteritic Posterior Ischemic Optic Neuropathy with Atypical Recovery Secondary to Biologically Occult Giant Cell Arteritis: A Case Report
Introduction: Posterior ischemic optic neuropathy (PION) is a rare form of ischemic optic neuropathy, and arteritic PION secondary to giant cell arteritis (GCA) usually has a poor prognosis. Case Presentation: We report a rare case of probable arteritic PION secondary to GCA with an atypically slow…
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Artikel Jurnal
High-Pressure Water Jet Ocular Injuries during Riot Control: A Case Series
Introduction: Eye injuries caused by a high-pressure water jet are rarely reported and mostly occur in sporadic trauma. This study aimed to describe various ocular injuries caused by water jets, with a particular emphasis on injuries inflicted by water cannon vehicles used during riots. Case…
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Artikel Jurnal
Progressive Visual Recovery in a Patient with Leber Hereditary Optic Neuropathy Harboring a Rare Heteroplasmic (MT-ND5):m.13042G>A, p(Ala236Thr) Variant with Low Mutant Load: A Case Report
Introduction: The majority of Caucasian patients with Leber hereditary optic neuropathy (LHON) harbor one of three primary pathogenic mitochondrial DNA (mtDNA) variants, which are usually present in homoplasmy in leukocytes. Most of the remaining cases have been linked to rare heteroplasmic…
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Artikel Jurnal
Spontaneous Orbital Wall Fracture Secondary to Neglected Graves’ Orbitopathy: A Case Report and Review of Current Literature
Introduction: Spontaneous orbital wall fracture, or bony auto-decompression, is an uncommon manifestation of advanced thyroid eye disease (TED) and results from chronic intraorbital hypertension driven by extraocular muscle hypertrophy. Case Presentation: We report a 72-year-old woman with a…
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Artikel Jurnal
Annulated Surprise during Cataract Surgery: A Case Report
Introduction: We report a pediatric case in which a retrolenticular Armillifer armillatus infestation mimicked a white cataract. Case Presentation: A ten-year-old girl presented with a white cataract of her right eye during a humanitarian mission in the Democratic Republic of Congo. Fundoscopy was…
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Artikel Jurnal
Bilateral Acanthamoeba Keratitis secondary to contaminated contact lens suction applicators: A rare case of accessory-mediated transmission
Background: Acanthamoeba keratitis (AK) is a sight-threatening corneal infection primarily associated with contact lens wear. While lens and case hygiene are frequently emphasised, auxiliary tools such as suction applicators remain a neglected vector for transmission. This report highlights a case…
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Artikel Jurnal
Novel Variants in Mitochondrial Ribosomal RNA Genes MT-RNR1 and MT-RNR2 Identified In Hereditary Optic Neuropathy Initially Presenting as Normal Tension Glaucoma: A Case Report
Introduction: Hereditary optic neuropathy may be caused by various mitochondrial or nuclear DNA mutations affecting the mitochondrial function. A growing body of evidence shows that mutations in nonclassical mitochondrial genes, including the ribosomal RNA genes MT-RNR1 and MT-RNR2, have been…
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Artikel Jurnal
Optic Perineuritis Mimicking Optic Nerve Sheath Meningioma: A Case Series
Introduction: Optic perineuritis (OPN) can mimic optic nerve sheath meningioma (ONSM) both clinically and radiographically, which may lead to misdiagnosis and inappropriate treatment. Case Presentations: We describe two cases of autoimmune-related OPN that were initially presumed to be ONSM. The…
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Artikel Jurnal
A Rare Septuagenarian Patient with a Mild Form of Mucopolysaccharidosis Type IIIC with Ocular Manifestations, a Case Report
Purpose: We present an atypical case of mucopolysaccharidosis (MPS) type IIIC to contribute to the growing understanding of its clinical heterogeneity and expand the known phenotypic spectrum of the disorder. This report describes one of the oldest known patients with genetically confirmed MPS…
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Artikel Jurnal
FLVCR1 Variant as a Cause of Retinal and Neurologic Dysfunction in Retinitis Pigmentosa with Coats-Like Vasculopathy: A Case Report
Purpose: We report a unique clinical presentation of a patient with undiagnosed neurologic symptoms in the setting of retinitis pigmentosa (RP) with Coats-like reaction and FLVCR1 mutation, expanding the presentation of FLVCR1 variants. Case: A 31-year-old Caucasian female with RP with Coats-like…
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Artikel Jurnal
DUAL ETIOLOGY IN OPTIC DISC ELEVATION: A PEDIATRIC CASE WITH COEXISTING OPTIC DISC DRUSEN AND ELEVATED CEREBROSPINAL FLUID PRESSURE
Purpose: In the presence of bilateral optic disc elevation with supportive clinical findings, papilledema should be considered the primary diagnosis. Particularly in bilateral presentations, optic disc drusen must be carefully evaluated in the differential diagnosis. The coexistence of these…
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Artikel Jurnal
Reactivation of Varicella-Zoster Virus Keratitis after Recombinant Herpes Zoster Vaccination: A Case Report and Literature Review
Introduction: VZV keratitis following recombinant herpes zoster vaccination is rare, and its underlying mechanisms remain poorly understood. Sporadic cases of ocular inflammatory reactivation have been reported after vaccination, particularly in patients with a history of herpes zoster infection…
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Artikel Jurnal
Clinical Insights and Genetic Implications: "A Comprehensive Case Series of Two Siblings with Cohen Syndrome"
Background: Cohen syndrome is a rare autosomal recessive developmental disorder with various clinical manifestations. These include failure to thrive, hypotonia, intellectual disability, pigmentary retinopathy, myopia, nyctalopia, microphthalmia, acquired microcephaly, truncal obesity, joint…
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Artikel Jurnal
Ocular Bartonellosis with Rapidly Progressive Choroidal Granuloma: Case Report
Ocular bartonellosis most commonly presents as neuroretinitis, whereas choroidal granulomas are rare and poorly characterized. This case highlights a rapidly progressive, tumor-mimicking choroidal granuloma, expanding the clinical spectrum, and highlights the importance of early recognition. A…
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Artikel Jurnal
Post-dural puncture headache with abducens nerve palsy after epidural labor analgesia: successful treatment with CT-guided epidural blood patch. A case report.
Post-dural puncture headache (PDPH) is a well-recognized complication of neuraxial anesthesia caused by cerebrospinal fluid (CSF) leakage and intracranial hypotension. Although usually self-limiting, persistent PDPH may rarely be complicated by cranial nerve palsy. We report the case of a…
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Artikel Jurnal
Acute unilateral NAION following tirzepatide therapy: a case report
Introduction: Dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonists, such as tirzepatide, have significantly advanced the management of type 2 diabetes mellitus and obesity. However, emerging safety signals have raised concerns regarding rare…
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Artikel Jurnal
Axial length–driven anisometropia in cornea plana spectrum with alternating exotropia
Cornea plana is a rare congenital corneal disorder characterised by marked corneal flattening, often with microcornea and shallow anterior chambers. It is classically associated with high hyperopia and accommodative esotropia. We report a 35-year-old woman with a cornea plana spectrum phenotype in…
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