نتایج جستجو برای: hereditary lens subluxation

تعداد نتایج: 136766  

Journal: :Journal of cataract and refractive surgery 2011
Samantha R De Silva Kikkeri Arun Maghizh Anandan Nicholas Glover Chetan K Patel Paul Rosen

PURPOSE To evaluate the indications, postoperative visual efficacy, and complication rate after intraocular implantation of an iris-claw aphakic intraocular lens (IOL). SETTING Oxford Eye Hospital, Oxford, United Kingdom. DESIGN Case series. METHODS This chart review comprised eyes with no capsule support that had anterior iris-fixation IOL implantation for aphakia between 2001 and 2009. ...

2013
Yong Joon Kim Seung Joo Ha

PURPOSE To report a case of pupillary block glaucoma associated with spontaneous crystalline lens subluxation into the anterior chamber in a 34-year-old man. METHODS Dry vitrectomy was performed for securing enough retrolental space, and an intracapsular lens extraction was then performed via a corneolimbal incision. Additional endothelial cell damage was avoided with an injection of viscoela...

Journal: :The Journal of the American Academy of Orthopaedic Surgeons 2005
Jonathan R Stieber John P Dormans

The solitary osteochondroma, a common pediatric bone tumor, is a cartilage-capped exostosis. Hereditary multiple exostosis is an autosomal dominant disorder manifested by the presence of multiple osteochondromas. Linkage analysis has implicated mutations in the EXT gene family, resulting in an error in the regulation of normal chondrocyte proliferation and maturation that leads to abnormal bone...

Journal: : 2022

Traumatic eyeball damages is a topical issue in present-day ophthalmology as they constitute one of the main causes vision loss people working age. Purpose: to assess feasibilty, effectiveness and safety one-time early-stage microinvasive optical reconstructive surgery patient with traumatic damage consequences: swelling cataract, lens ligamentous apparatus defect, iridodialysis, mydriasis. Mat...

Journal: :The British journal of ophthalmology 2000
A D Mumford I A Cree J D Arnold M C Hagan K C Rixon J J Harding

BACKGROUND/AIM Hereditary hyperferritinaemia cataract syndrome (HHCS) is an autosomal dominant disorder characterised by elevated serum L-ferritin and bilateral cataracts. The ocular manifestations of this disorder are poorly studied. This study therefore sought to determine the origin of cataracts in HHCS. METHODS L-ferritin ELISA, immunohistochemical and ultrastructural analysis of a lens n...

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