Results 31 to 40 of about 17,930 (224)
Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy [PDF]
, 2014 Exome sequencing revealed a homozygous missense mutation (c.317C>G [p.Arg106Pro]) in POC1B, encoding POC1 centriolar protein B, in three siblings with autosomal-recessive cone dystrophy or cone-rod dystrophy and compound-heterozygous POC1B mutations (c ...
Arts, Heleen H +17 more
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Nanophthalmos and situs inversus totalis
Indian Journal of Ophthalmology, 2012 Nanophthalmos is characterized by short axial length, high hypermetropia, thick sclera and a normal-sized crystalline lens. Situs inversus totalis is the mirror image of the normal morphology of the thoracic and abdominal viscera.
Alparslan Sahin +3 more
doaj +1 more source
Acute macular neuroretinopathy associated with intravitreal anti-VEGF injection: A case report
American Journal of Ophthalmology Case Reports, 2022 Purpose: to report a case of acute macular neuroretinopathy occurring after intravitreal aflibercept injection for macular edema due to CRVO. Observations: Two days after Aflibercept intravitreal injection, the patient developed vision loss associated ...
Loubna M. Radwan +3 more
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Medical management of hereditary optic neuropathies. [PDF]
, 2014 Hereditary optic neuropathies are diseases affecting the optic nerve. The most common are mitochondrial hereditary optic neuropathies, i.e., the maternally inherited Leber's hereditary optic neuropathy (LHON) and dominant optic atrophy (DOA).
Barboni, Piero +4 more
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Electrophysiological abnormalities associated with extensive myelinated retinal nerve fibers
Indian Journal of Ophthalmology, 2012 An observational case report of electrophysiological abnormalities in a patient with anisomyopic amblyopia as a result of unilateral extensive myelinated retinal nerve fibers (MNFs) is illustrated.
Su Ann Tay, Srinivasan Sanjay
doaj +1 more source
Indian Journal of Ophthalmology, 2012 We report a case of isolated homonymous hemianopsia due to presumptive cerebral tubercular abscess as the initial manifestation of human immunodeficiency virus (HIV) infection.
Sujit Gharai +4 more
doaj +1 more source
Occult macular dystrophy in an Italian family carrying a mutation in the RP1L1 gene. [PDF]
, 2016 Occult macular dystrophy (OMD) is an inherited macular disease characterized by progressive visual decline with the absence of visible retinal abnormalities. Typical alterations of the retinal structure are detectable by spectral domain optical coherence
Colavito, Davide +4 more
core +1 more source
Functional evaluation of the macular area in early glaucoma using microperimetry
Indian Journal of Ophthalmology, 2021 Purpose: To evaluate the central visual field by microperimetry (MP), in early glaucoma. Methods: Consecutive perimetrically experienced patients with a single nasal step or arcuate scotoma and 14 control eyes underwent MP.
Swati Phuljhele +6 more
doaj +1 more source
Clues from Crouzon: Insights into the potential role of growth factors in the pathogenesis of myelinated retinal nerve fibers. [PDF]
, 2016 PurposeWe present a case of bilateral extensive peripapillary myelinated retinal nerve fibers (MRNF) in an individual with Crouzon syndrome, an inherited form of craniosynostosis caused by overactivation of fibroblast growth factor receptor 2.
Akil, Handan +5 more
core +3 more sources
Homonymous hemianopsia: Case report [PDF]
ABC: časopis urgentne medicine, 2018 Introduction: Cerebrovascular diseases include a wide range of diseases and disorders based on damage to the blood vessels of the brain. Disorders in the visual field can be caused by various neurological and ocular diseases.
Repac Vinka J. +2 more
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