A. Chebil
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View article: Epidemiology and Visual Outcome of Pediatric Ocular Trauma in a Major Tertiary Eye Center in Tunisia: A 6-Year Retrospective Study
Epidemiology and Visual Outcome of Pediatric Ocular Trauma in a Major Tertiary Eye Center in Tunisia: A 6-Year Retrospective Study Open
Purpose: To describe the epidemiological profile, clinical characteristics, and visual outcome of pediatric ocular trauma in Tunisia. Methods: In this retrospective cohort study, we reviewed the charts of 398 children younger than 16 years…
View article: Occlusive retinal vasculopathy following AstraZeneca COVID-19 vaccination: A case report
Occlusive retinal vasculopathy following AstraZeneca COVID-19 vaccination: A case report Open
View article: Management of a Bilateral Post-Uveitic Complex Glaucoma with Pupillary Block, Rupture of the Anterior Lens Capsule, and Malignant Glaucoma Following Laser Peripheral Iridotomies
Management of a Bilateral Post-Uveitic Complex Glaucoma with Pupillary Block, Rupture of the Anterior Lens Capsule, and Malignant Glaucoma Following Laser Peripheral Iridotomies Open
Purpose: To report a case of a bilateral complex uveitic glaucoma (UG) with pupillary block, rupture of the anterior lens capsule, and malignant glaucoma in a young high-myopic patient and to report anterior segment optical coherence tomog…
View article: Contribution of ultra-wide field fluorescein angiography in diabetic retinopathy in a Tunisian population.
Contribution of ultra-wide field fluorescein angiography in diabetic retinopathy in a Tunisian population. Open
UWF-FA was of great help assessing DR and evaluating peripheral retinal lesions in order to refine DR staging and to guide laser treatment. Besides, it allows better understanding of DME pathophysiology.
View article: Swept Source Optical Coherence Tomography Angiography: Characteristic Findings in Type 3 Macular Neovascularization.
Swept Source Optical Coherence Tomography Angiography: Characteristic Findings in Type 3 Macular Neovascularization. Open
We report a typical illustration of Swept source OCT-Angiography (SS-OCT-A) findings in type 3 macular neovascularization(MNV) or retinal angiomatous proliferation (RAP). This is a case of a 70-year-old Caucasian male patient presenting wi…
View article: Apocrine hidrocystoma of the orbit mimicking basal cell carcinoma: a case report
Apocrine hidrocystoma of the orbit mimicking basal cell carcinoma: a case report Open
Apocrine hidrocystomas are benign cystic lesions derived from the sweat glands. They are rarely seen in the orbit with very few adult cases published in literature. We present a case of a 40-year-old female, with no prior medical history o…
View article: Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography
Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography Open
Purpose: We report the case of a neurologically asymptomatic young boy presenting with an unusual phenotype of CYP2U1 related macular dystrophy associating bilateral macular telangiectasia (MacTel) and fibrotic choroidal neovascularization…
View article: Acute macular outer retinopathy as a presumed manifestation of COVID-19
Acute macular outer retinopathy as a presumed manifestation of COVID-19 Open
View article: OCT-angiography assessing quiescent and active choroidal neovascularization in retinitis pigmentosa associated with <i>PRPH2</i> pathogenic variant
OCT-angiography assessing quiescent and active choroidal neovascularization in retinitis pigmentosa associated with <i>PRPH2</i> pathogenic variant Open
Purpose: To report multimodal imaging findings including optical coherence tomography angiography (OCT-A) of a patient presenting with a quiescent choroidal neovascularization (CNV) in one eye and an active CNV in the fellow eye, complicat…
View article: Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies
Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies Open
Retinal dystrophies (RD) are a group of Mendelian disorders caused by rare genetic variations leading to blindness. A pathogenic variant may manifest in both dominant or recessive mode and clinical and genetic heterogeneity makes it diffic…
View article: Central corneal thickness in a healthy Tunisian population.
Central corneal thickness in a healthy Tunisian population. Open
The normal CCT value in the Tunisian population was of 522±37.17 µm. We have analyzed, for the first time, normal central corneal thickness values of a healthy Tunisian population.
View article: Homozygous mutation in ABCA4 associated with cone rod dystrophy in a patient with Turner syndrome.
Homozygous mutation in ABCA4 associated with cone rod dystrophy in a patient with Turner syndrome. Open
Several ocular disorders are known to be associated with Turner syndrome, however, in this case, we hypothesize that CRD is not related to Turner syndrome but may be a manifestation of the lack of a normal X chromosome with ABCA4 mutation.
View article: E-learning for Ophthalmology Training Continuity During COVID-19 Pandemic: Satisfaction of residents of Hédi Raies Institut of Ophthalmology of Tunis.
E-learning for Ophthalmology Training Continuity During COVID-19 Pandemic: Satisfaction of residents of Hédi Raies Institut of Ophthalmology of Tunis. Open
This study highlights the importance of virtual learning in ophthalmology in the era of the COVID-19 pandemic. E-learning is well appreciated by ophthalmology residents, relatively easy to integrate to their training program, and reduces i…
View article: Sulodexide for Diabetic-Induced Disabilities: A Systematic Review and Meta-Analysis
Sulodexide for Diabetic-Induced Disabilities: A Systematic Review and Meta-Analysis Open
View article: Subthreshold micropulse laser adjuvant to bevacizumab versus bevacizumab monotherapy in treating diabetic macular edema: one- year- follow-up
Subthreshold micropulse laser adjuvant to bevacizumab versus bevacizumab monotherapy in treating diabetic macular edema: one- year- follow-up Open
Purpose: To compare the therapeutic impact of combining intravitreal injections of bevacizumab (IVB) with micropulse laser (MPL) in central diffuse diabetic macular edema (DME) versus IVB monotherapy during 12 months follow-up. Methods: We…
View article: Genetic spectrum of retinal dystrophies in Tunisia
Genetic spectrum of retinal dystrophies in Tunisia Open
View article: Multimodal Imaging in Retinitis Pigmentosa
Multimodal Imaging in Retinitis Pigmentosa Open
Purpose: To analyze microvascular changes in patients with retinitis pigmentosa (RP) with relatively preserved visual acuity (VA), using swept source optical coherence tomography (SS-OCT) angiography to correlate results to macular functio…
View article: Optical coherence tomography angiography of a bilateral optic disc pit
Optical coherence tomography angiography of a bilateral optic disc pit Open
Optic disc pit (ODP) is a rare congenital defect presumably arising from the failure of fetal fissure closure in embryogenesis. It occurs in about 1 in 10,000 people with no gender predilection. ODP is usually unilateral. We describe the c…
View article: Macular Microvascular Changes in Patients With Retinitis Pigmentosa Using Optical Coherence Tomography Angiography: correlation to macular structure and function
Macular Microvascular Changes in Patients With Retinitis Pigmentosa Using Optical Coherence Tomography Angiography: correlation to macular structure and function Open
View article: Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New <i>ABCA4</i> Mutations
Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New <i>ABCA4</i> Mutations Open
To assess the progression of Stargardt (STGD) disease over nine years in two branches of a large consanguineous Tunisian family. Initially, different phenotypes were observed with clinical intra- and interfamilial variations. At presentati…
View article: Novel RPGRIP1 mutation in Leber congenital amaurosis patients
Novel RPGRIP1 mutation in Leber congenital amaurosis patients Open
View article: Correction: Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy
Correction: Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy Open
Scientific Reports 6: Article number: 37455; published online: 22 November 2016; updated: 04 May 2017 This Article contains errors. The position of the mutation p.(R91W); (V172D) was incorrectly calculated, taking as a starting point the b…
View article: Exome sequencing confirms <i>ZNF408</i> mutations as a cause of familial retinitis pigmentosa
Exome sequencing confirms <i>ZNF408</i> mutations as a cause of familial retinitis pigmentosa Open
Retinitis pigmentosa (RP), a hereditary retinal disorder causing degeneration of photoreceptors,1,2 displays large heterogeneity in terms of clinical manifestations, hereditary pattern, and causati...
View article: Identifying mutations in Tunisian families with retinal dystrophy
Identifying mutations in Tunisian families with retinal dystrophy Open
View article: Optical Coherence Tomographic Findings in Berlin’s Edema
Optical Coherence Tomographic Findings in Berlin’s Edema Open
Purpose: To describe optical coherence tomography (OCT) findings in a patient with Berlin’s edema following blunt ocular trauma. Case Report: A 26-year-old man presented with acute loss of vision in his left eye following blunt trauma. He …
View article: Corrélations phénotype–génotype de la rétinopathie pigmentaire non syndromique : à propos de dix familles tunisiennes
Corrélations phénotype–génotype de la rétinopathie pigmentaire non syndromique : à propos de dix familles tunisiennes Open
View article: Purtscher-like retinopathy as a rare presentation of cryoglobulinemia
Purtscher-like retinopathy as a rare presentation of cryoglobulinemia Open
Purtscher's retinopathy is a rare condition that is noted in cases related to various types of trauma. The characteristic finding in the fundus is the presence of multiple Purtscher flecken. Purtscher-like retinopathy has a similar present…
View article: Current and emerging treatment options for myopic choroidal neovascularization
Current and emerging treatment options for myopic choroidal neovascularization Open
Choroidal neovascularization (CNV) is the main cause of visual impairment in highly myopic patients younger than 50 years of age. There are different treatments for myopic CNV (mCNV), with 5- to 10-year outcomes currently. Chorioretinal at…
View article: Characteristics of astigmatism in a population of Tunisian school-children
Characteristics of astigmatism in a population of Tunisian school-children Open
Comparisons with other studies show that the prevalence of astigmatism in Tunisia is higher than in some countries. The prevalence of astigmatism increased with age but not gender. The majority of schoolchildren had with-the-rule astigmati…