Amniotic membrane placement without endotamponade for optic nerve coloboma with extensive serous retinal detachment in papillorenal syndrome: A case report [PDF]
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]
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]
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]
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]
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
Juxtapapillary retinochoroidal coloboma presenting with macular retinoschisis
Raj S Hirawat, C K Nagesha, M Arthi
doaj +3 more sources
Unilateral macular Coloboma: a rare finding. [PDF]
Moutei H +4 more
europepmc +2 more sources
Bilateral congenital macular coloboma: a case report. [PDF]
Feng C, Li H.
europepmc +2 more sources
Expanded Phenotype of PAX2-Related Papillorenal Syndrome: A Case Featuring FSGS, Atypical Retinopathy, Cerebellar Hypoplasia, and ADHD. [PDF]
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
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

