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FLACS (Femtosecond-Laser-Assisted Cataract Surgery) combined with pupiloplasty in iris-lens coloboma [PDF]

open access: yesAmerican Journal of Ophthalmology Case Reports
Purpose: To describe the use of FLACS (Femtosecond-Laser-Assisted Cataract Surgery) and pupiloplasty technique employed in a cataract surgery associated with iris-lens-zonule coloboma, as well as to report the advantages that FLACS can provide in this ...
Cristian Fernández-Martínez
exaly   +4 more sources

Diverse presentations of ectopia lentis and lens coloboma in Marfan's syndrome

open access: yesOman Journal of Ophthalmology, 2023
Marfan's syndrome (MFS) is an autosomal dominant connective tissue disorder with defect in the fibrillin-1 gene. The most common ocular manifestation is subluxated lens in the superotemporal direction, accounting for 50%–85% of total cases.
Richa Dhiman   +3 more
doaj   +2 more sources

Bilateral Toric Phakic Intraocular Lens Implantation for Correction of High Myopic Astigmatism in a Patient with Marfan Syndrome with Lens Coloboma: A Case Report [PDF]

open access: yesCase Reports in Ophthalmology, 2021
Marfan syndrome (MFS) is known to cause significant refractive error. Treatment options are limited in this condition for correcting refractive error. Clear lens exchange is done in these cases, but complication rates are high.
Bhupesh Singh   +4 more
doaj   +2 more sources

Bilateral ectopia lentis with isolated lens coloboma in Marfan syndrome [PDF]

open access: yesGMS Ophthalmology Cases, 2016
A rare case of bilateral ectopia lentis with isolated lens coloboma in Marfan syndrome is reported. A 21-year-old female presented with decreased vision in both eyes. Her unaided visual acuity was 20/200 and 20/400 in the right and left eye, respectively,
Sahu, Sabin   +3 more
doaj   +2 more sources

Surgical Management and Scheimpflug Analysis of an Atypical Lens Coloboma [PDF]

open access: yesCase Reports in Ophthalmology, 2012
A lens coloboma is not a true coloboma; it is just a zonular absence that causes a defect in the lens equator and hence a more spherical lens. It can be isolated or in association with iris, choroid or retinal colobomas.
Julio C. Hernadez-Camarena   +3 more
doaj   +2 more sources

Superior Lens Coloboma with Superior Rectus Palsy and Congenital Ptosis

open access: yesJournal of Optometry, 2009
A lens coloboma is characterized by the lens tissue's notching at the equator. It is usually inferior-nasal else it is called an atypical coloboma. We report a young male who presented with a superior lens coloboma, an elevation deficit and moderate ...
Jitendra Jethani
exaly   +3 more sources

An unusual case of iris and lens colobomas: A case report [PDF]

open access: yesTherapeutic Advances in Ophthalmology
Ocular colobomas are unusual congenital anomalies arising from abnormal ocular development and may involve different ocular structures, including the iris and lens.
Cong Ren   +5 more
doaj   +2 more sources

Bilateral Eyelid Agenesis With Multiple Congenital Ocular Anomalies in an Australian Labradoodle Puppy: Case Report and Surgical Management. [PDF]

open access: yesVet Ophthalmol
ABSTRACT A 15‐week‐old Australian Labradoodle puppy was presented to The University of Queensland Small Animal Hospital for bilateral eyelid agenesis/coloboma and associated ocular complications. Enucleation of the left globe and repair of the right eyelid via a lip‐to‐lid transmucosal flap was performed. Given the subsequent development of prolapse of
Ng CH   +4 more
europepmc   +2 more sources

Case Report: Persistent fetal vasculature associated with lenticular coloboma [PDF]

open access: yesFrontiers in Medicine
BackgroundPersistent fetal vasculature (PFV) is a rare congenital ocular anomaly, featuring typical fibrovascular stalks in the vitreous cavity.
Naiyu Sun, Jinchang Tian, Hong Zhang
doaj   +2 more sources

CHARGE Syndrome Associated With Persistent Hyperplastic Primary Vitreous: A Case Report. [PDF]

open access: yesCase Rep Ophthalmol Med
Background CHARGE syndrome is a rare genetic disorder caused primarily by CHD7 mutations, affecting multiple organs, including the eyes, heart, and ears. Ocular abnormalities are common, but bilateral persistent fetal vasculature (PFV) has not been previously reported in CHARGE syndrome.
Liu L   +7 more
europepmc   +2 more sources

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