Results 11 to 20 of about 3,780 (251)

Optic Disc Imaging by Heidelberg Retinal Tomogram in Congenital Optic Disc Anomaly

open access: yesIndian Journal of Ophthalmology, 2004
We evaluated two cases of congenital optic disc anomaly with the Heidelberg Retinal Tomograph (HRT) that could be mistaken for glaucomatous optic disc. One was an optic disc coloboma with a visual field defect and the other had an optic disc pit without ...
Kunjam Vallam, Sekhar G
doaj   +2 more sources

Clinical features of strabismus in patients with congenital optic disc anomaly. [PDF]

open access: yesKorean J Ophthalmol, 2021
To investigate the clinical features of strabismus in patients with congenital optic disc anomaly and compare and analyze the characteristics of patients who showed changes in the strabismus pattern with those who did not.Medical records of the patients who were diagnosed with both strabismus and congenital optic disc anomaly and followed-up for ≥1 ...
Jeon H, Jo Y, Choi HY.
europepmc   +4 more sources

Diagnostic dilemma: Morning glory disc anomaly or optic disc pit?

open access: yesIndian Journal of Ophthalmology. Case Reports, 2023
Megha B Patel   +5 more
doaj   +2 more sources

Twin disc anomaly – A rare case of optic disc pit with disc coloboma

open access: yesIndian Journal of Ophthalmology. Case Reports, 2023
Gulshan Barwar   +3 more
doaj   +2 more sources

Combined cavitary anomalies of the optic disc with maculopathy [PDF]

open access: yesBMJ Case Reports, 2021
Cavitary optic disc anomalies can cause maculopathy. The most common of these associated with maculopathy is the optic disc pit. Very rarely, maculopathy can accompany optic disc coloboma. We report a case of combined cavitary disc anomalies (coloboma and disc pit) with maculopathy.
Hirawat Rajshri   +2 more
openaire   +2 more sources

Optic disc anomalies and frontonasal dysplasia [PDF]

open access: yesBritish Journal of Ophthalmology, 1998
To document the optic disc abnormalities in patients with frontonasal dysplasia in association with basal encephalocele.Names and hospital numbers of patients with midline clefts were obtained from the ophthalmology and genetics database. Six patients were identified who had the following common findings: midline facial cleft with midline cleft lip and
P, Hodgkins   +7 more
openaire   +2 more sources

A Rare Case Report of Morning Glory Syndrome in North Karnataka, Vijayapura

open access: yesBLDE University Journal of Health Sciences, 2020
Background: Morning Glory Syndrome is a rare congenital optic disc anomaly. The etiology of the disorder remains controversial and unclear. It is uncommon and can be either isolated or associated with malformations.
Sunil Biradar, Magna Mary Kuruvila
doaj   +1 more source

Historical aspects and current views of the etiopathogenesis and clinical manifestations of optic nerve pits

open access: yesРоссийский офтальмологический журнал, 2022
Optic nerve pits are a mono- or bilateral congenital anomaly represented by optic disc depressions of various sizes. In half of the cases, the pits are complicated by edema, central retinal detachment and retinoschisis, and cause visual function decrease.
E. V. Muskatina   +3 more
doaj   +1 more source

Optic Disc Anomalies with Excavation in the Disc (Optic Disc Pit, Morning Glory Disc Anomaly, Optic Disc Coloboma, Peripapillary Staphyloma)

open access: yesGüncel Retina Dergisi (Current Retina Journal), 2022
Optic disc pits, optic disc coloboma, morning glory disc anomaly, and peripapillary staphyloma are the leading optic disc anomalies with excavation in the disc. These anomalies can be seen together with some syndromes and in this case, can be evaluated as part of the spectrum of the disease.
openaire   +1 more source

Management of double optic disc pit complicated by maculopathy

open access: yesIndian Journal of Ophthalmology, 2020
Optic disc pit (ODP) is a rare, congenital, cavitary anomaly of the optic disc. Usually, single ODP occurs in an eye and only eleven cases of double ODP have been reported so far in the literature.
Naresh Babu   +3 more
doaj   +1 more source

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