Results 1 to 10 of about 2,217 (192)

Bilateral Hypertensive Papillopathy with Diffuse Retinal Telangiectasis. [PDF]

open access: yesBeyoglu Eye J, 2022
A 16-year-old type 1 diabetic female patient was consulted to our clinic for acute bilateral painless vision loss with a 2-week history in the right eye and a 1-week history in the left eye. At the initial visit, the best-corrected visual acuity was 0.2 in the right eye and 0.05 in the left eye.
Limon U, Akcay BIS.
europepmc   +3 more sources

Idiopathic Juxtafoveolar Retinal Telangiectasis

open access: yesDelhi Journal of Ophthalmology, 2010
Idiopathic juxtafoveolar retinal telangiectasis (IJRT), also known as idiopathic macular telangiectasia (IMT), refers to a heterogeneous group of well recognized clinical entities characterized by telangiectatic alterations of the juxtafoveolar capillary
Neha Goel   +4 more
doaj   +4 more sources

Multimodal Imaging Characteristics in Unilateral Occlusive Macular Telangiectasia with Atypical X-Shaped Lesion [PDF]

open access: yesDiagnostics
Macular Telangiectasia (MacTel) is a rare retinal vascular disorder, with Type 3a MacTel being a distinct form characterized by retinal ischemia with the classical findings of MacTel, such as juxtafoveal telangiectasis, right-angled venules, and deep ...
Abdullah Ağın   +2 more
doaj   +2 more sources

Idiopathic juxtafoveolar retinal telangiectasis: a current review.

open access: yesMiddle East Afr J Ophthalmol, 2010
Idiopathic juxtafoveolar retinal telangiectasis (IJFT), also known as parafoveal telangiectasis or idiopathic macular telangiectasia, refers to a heterogeneous group of well-recognized clinical entities characterized by telangiectatic alterations of the juxtafoveolar capillary network of one or both eyes, but which differ in appearance, presumed ...
Nowilaty SR, Al-Shamsi HN, Al-Khars W.
europepmc   +4 more sources

Adult Coats’ Disease Successfully Managed with the Dexamethasone Intravitreal Implant (Ozurdex®) Combined with Retinal Photocoagulation [PDF]

open access: yesCase Reports in Ophthalmology, 2012
Purpose: To report a case of Coats’ disease managed with the dexamethasone intravitreal implant Ozurdex® (Allergan, Inc., Irvine, Calif., USA) combined with retinal photocoagulation.
Sebastián Martínez-Castillo   +4 more
doaj   +4 more sources

Idiopathic juxtafoveolar retinal telangiectasis in monozygotic twins. [PDF]

open access: yesBr J Ophthalmol, 2007
Monozygotic twins (aged 63 years old), with group-2A idiopathic juxtafoveolar retinal telangiectasia (JXT), underwent clinical examination, fluorescein angiography (FA) and optical coherence tomography (OCT). Twin 1 : Right fundus showed right-angled venules temporal to the fovea; FA demonstrated retino-retinal anastomosis and intraretinal leakage ...
Hannan SR   +3 more
europepmc   +5 more sources

Place of dexamethasone implant as an adjunctive treatment in Coats’ disease: a retrospective single-center study [PDF]

open access: yesBMC Ophthalmology
Background To evaluate the efficacy and safety of intravitreal dexamethasone implant as an adjunctive treatment to ablative therapy in Coats’ disease.
Ozlem Ural Fatihoglu   +5 more
doaj   +2 more sources

Telangiectasia retiniana parafoveal unilateral Unilateral parafoveal retinal telangiectasis

open access: yesRevista Brasileira de Oftalmologia, 2007
Telangiectasia retiniana é um termo inicialmente proposto por Reese, em 1956. Caracteriza-se por uma anormalidade vascular retiniana, com dilatação irregular e incompetência dos vasos.
Mário Martins dos Santos Motta   +1 more
doaj   +2 more sources

High-Resolution Imaging in Macular Telangiectasia Type 2: Case Series and Literature Review [PDF]

open access: yesDiagnostics
Background: Macular telangiectasia (MacTel), also known as idiopathic juxtafoveolar telangiectasis (IJFTs), involves telangiectatic changes in the macular capillary network.
Andrada Elena Mirescu   +7 more
doaj   +2 more sources

Central nervous system anomalies in 41 Chinese children incontinentia pigmenti [PDF]

open access: yesBMC Neuroscience
Introduction Incontinentia pigmenti (IP) is a rare neuroectodermal dysplasia caused by a defect in the IKBKG gene. The pathogenesis of central nervous system injury is believed to be related to microvascular ischemia.
Li Yin   +6 more
doaj   +2 more sources

Home - About - Disclaimer - Privacy