scholarly journals Clinical features of strabismus in patients with congenital optic disc anomaly

2021 ◽  
Vol 35 (2) ◽  
pp. 136-141
Author(s):  
Hyeshin Jeon ◽  
Yeonji Jo ◽  
Hee-young Choi
2015 ◽  
Vol 159 (5) ◽  
pp. 973-979.e2 ◽  
Author(s):  
Cecilie Bredrup ◽  
Stefan Johansson ◽  
Laurence A. Bindoff ◽  
Pawel Sztromwasser ◽  
Jostein Kråkenes ◽  
...  

2005 ◽  
Vol 36 (5) ◽  
pp. 374-380 ◽  
Author(s):  
Ingrid U Scott ◽  
Harry W Flynn Jr ◽  
Luma Al-Attar ◽  
Gail L Ganser ◽  
Antonio V Aragon ◽  
...  

Author(s):  
Peter A. Quiros ◽  
Alfredo A. Sadun

In this chapter, we discuss inherited/congenital optic nerve diseases and their related visual fields defects. It is important for the ophthalmologist to establish, on the basis of the visual fields defect whether the optic nerve is involved and, if so, whether this is at the level of the optic disc or further back. In addition, the visual fields defect can help establish whether the etiology is acquired or congenital. If the former is the case, then the visual fields defect may reveal an insult that is rapidly progressive and hence requires immediate and aggressive management. The diseases are divided into the categories of congenital optic disc anomalies and heredodegenerative optic atrophies. Congenital optic disc anomalies include aplasias, dysplasias (hyperplasia and hypoplasia), optic nerve colobomas and pits, anomalous disc elevations: pseudopapilledema with or without hyaline bodies (drusen), and tilted disc and crescents. Absence of the optic disc (aplasia) is extremely rare and only a few case reports have been published in the literature. Optic disc size varies and may be larger (hyperplasia) or smaller (hypoplasia) than normal. Hyperplasia is much less common than hypoplasia and is usually related to ametropias. Optic nerve hypoplasia (ONH) may be unilateral or bilateral and isolated or associated with different syndromes. It may be associated with good or poor visual prognosis. It is the most common congenital optic disc anomaly encountered in pediatric ophthalmic practice. When the nerve head is slightly or segmentally reduced, especially in the presence of normal visual acuity, the diagnosis is based on comparison of disc photographs or calculation of the ratio of the disc center-to-fovea distance to disc diameter. Usually this ratio is increased in hypoplasia and, if higher than 3.0, is almost diagnostic. Sometimes the hypoplastic disc is surrounded by a ring of sclera and a ring of hyperpigmentation, described as “double-ring sign”. Maternal diabetes and use of teratogenic agents such as phenytoin, alcohol, quinine, and cocaine may be associated with ONH.


2017 ◽  
Vol 39 (2) ◽  
pp. 271-274 ◽  
Author(s):  
Mohsin H. Ali ◽  
Nathalie F. Azar ◽  
Vinay Aakalu ◽  
Felix Y. Chau ◽  
Javaneh Abbasian ◽  
...  

2013 ◽  
Vol 33 (6) ◽  
pp. 721-724
Author(s):  
Dilek Güven ◽  
Nihal Balcıoğlu ◽  
Çağrı Türker ◽  
Yasemin Baydar ◽  
Yekta Şendül

2018 ◽  
Vol 2018 ◽  
pp. 1-12 ◽  
Author(s):  
Atsushi Tanaka ◽  
Wataru Saito ◽  
Satoru Kase ◽  
Kan Ishijima ◽  
Kousuke Noda ◽  
...  

Purpose. To evaluate the surgical outcomes of pars plana vitrectomy (PPV) with epipapillary membrane removal in patients with maculopathy associated with cavitary optic disc anomalies. Methods. Eight patients (8 eyes) with cavitary optic disc anomaly-associated maculopathy who underwent PPV with epipapillary membrane removal were retrospectively reviewed. The best-corrected visual acuity (BCVA) and macular and papillary morphologies using enhanced depth imaging optical coherence tomography (EDI-OCT) were evaluated before and after treatment. Immunohistochemistry for an intraoperatively excised epipapillary membrane tissue was also performed. Results. Before surgery, EDI-OCT revealed that epipapillary membrane was observed in all patients. Retinoschisis was resolved with no recurrence in all patients following vitrectomy regardless of a disease type or the presence or absence of preoperative posterior vitreous detachment. The mean final BCVA and central retinal thickness significantly improved compared with pretreatment values (P=0.008 and 0.004, resp.). Immunoreactivity for S100 protein and glial fibrillary acidic protein, markers of astrocytes, was positive in the resected membrane tissues. Conclusions. These results suggest that epipapillary membrane is involved in the pathogenesis of some patients with cavitary optic disc anomaly-associated maculopathy as well as posterior hyaloid membrane. PPV with epipapillary membrane removal may be a useful treatment option for this maculopathy. This trial is registered with UMIN000011123.


2013 ◽  
Vol 49 (6) ◽  
pp. 517 ◽  
Author(s):  
George N. Magrath ◽  
Edward W. Cheeseman ◽  
Robert A. Sarrica

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