Results 11 to 20 of about 3,282 (209)

Amniotic membrane placement without endotamponade for optic nerve coloboma with extensive serous retinal detachment in papillorenal syndrome: A case report [PDF]

open access: yesAmerican Journal of Ophthalmology Case Reports
Purpose: To report a rare case of serous macular detachment associated with optic nerve coloboma in a patient with genetically confirmed papillorenal syndrome, successfully treated with human amniotic membrane transplantation (hAMT) without endotamponade
Sara Lucchini   +5 more
doaj   +2 more sources

Late-Onset Subretinal Silicone Oil Migration through Optic Disc Coloboma [PDF]

open access: yesCase Reports in Ophthalmology
Introduction: This report describes a case of late onset subretinal silicone oil migration in an eye with congenital optic disc coloboma and its treatment.
Or Shmueli, Tareq Jaouni
doaj   +2 more sources

Hybrid cavitary disc anomaly – A case series and proposal of a novel classification system [PDF]

open access: yesIndian Journal of Ophthalmology
Background: Cavitary disc anomalies, including optic disc pit (ODP), optic nerve coloboma (ODC), and morning glory disc anomaly (MGDA), are congenital conditions with distinct embryological origins and systemic associations.
Savithiri Palanivel   +3 more
doaj   +2 more sources

Vitrectomy with amniotic membrane transplantation for macular choroidal coloboma with macular hole and posterior scleral staphyloma: a case report [PDF]

open access: yesFrontiers in Medicine
BackgroundThis study aimed to report a case of vitrectomy with amniotic membrane transplantation (AMT) for a macular choroidal coloboma (CC) associated with a macular hole (MH) and posterior scleral staphyloma (PSS).Case presentationA 54-year-old woman ...
Jie Liang   +3 more
doaj   +2 more sources

Optical coherence tomographic findings at the fixation point in a case of bilateral congenital macular coloboma [PDF]

open access: yesClinical Ophthalmology, 2014
Kosuke Abe,1,2 Jumi Shirane,2 Masuo Sakamoto,1 Fumi Tanabe,1 Kazuki Kuniyoshi,1 Chota Matsumoto,1 Yoshikazu Shimomura11Department of Ophthalmology, Kinki University Faculty of Medicine, Osaka-Sayama, Osaka, Japan; 2Nara Hospital, Kinki University Faculty
Abe K   +6 more
doaj   +2 more sources

Unilateral macular Coloboma: a rare finding. [PDF]

open access: yesOxf Med Case Reports
Moutei H   +4 more
europepmc   +2 more sources

Expanded Phenotype of PAX2-Related Papillorenal Syndrome: A Case Featuring FSGS, Atypical Retinopathy, Cerebellar Hypoplasia, and ADHD. [PDF]

open access: yesClin Case Rep
ABSTRACT Papillorenal syndrome (PAPRS), or renal coloboma syndrome, is a rare autosomal dominant disorder caused by PAX2 mutations. It classically manifests with renal hypodysplasia and optic nerve anomalies. However, recent literature suggests an expanding phenotypic spectrum.
Sultana N, Mamun AA, Begum A.
europepmc   +2 more sources

CHOROIDAL NEOVASCULARIZATION IN A CASE OF CHORIORETINAL COLOBOMA TREATED WITH INTRAVITREAL ANTI-VEGF INJECTONS: A CASE REPORT

open access: yesIJRETINA (International Journal of Retina), 2022
Introduction: Chorioretinal coloboma (CRC) results from abnormal closure of the embryonic fissure. Choroidal neovascularization (CNV) is a rare complication that associated with coloboma of the choroid.
Dicky Budiman Simanjuntak   +2 more
doaj   +1 more source

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