Results 21 to 30 of about 2,217 (192)

Clinical Studies into the Causes of Idiopathic Macular Telangiectasia Type 2: Sleep Apnoea and Macular Telangiectasia: The SAMTel Project [PDF]

, 2015
Purpose: To assess the prevalence of Obstructive Sleep Apnoea (OSA) in a population with Macular Telangiectasia Type 2 (MacTel) and how OSA impacts on MacTel progression.
Bovy, A.G., Groot, P.F.M., Jong, M de, Mariani, C., Powers, S.J., Rieu, I., Schimmel, B.C.J., Stultiens, C.L.M., Tikunov, Y.M., Vriezen, W.H., Wolters-Arts, M.   +10 more
core   +2 more sources

Adult onset coats disease in a 56-year-old male: An atypical presentation

Medical Journal of Dr. D.Y. Patil University, 2015
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remits and exacerbates throughout life. However, it is not rare for coats disease to present in adulthood for the first time.
Bodhraj Dhawan, Ankur Goel, Rajbir Singh, Vipan Vig   +3 more
doaj   +1 more source

Assessing Photoreceptor Structure Associated with Ellipsoid Zone Disruptions Visualized with Optical Coherence Tomography [PDF]

, 2016
Purpose: To compare images of photoreceptor layer disruptions obtained with optical coherence tomography (OCT) and adaptive optics scanning light ophthalmoscopy (AOSLO) in a variety of pathologic states.Methods: Five subjects with photoreceptor ellipsoid
Carroll, Joseph, Cooper, Robert F., Dubra, Alfredo, Flatter, John A., Han, Dennis P., Langlo, Christopher S., Neitz, Maureen, Pennesi, Mark E., Robison, Scott, Scoles, Drew, Weinberg, David V.   +10 more
core   +2 more sources

Multimodality imaging in macular telangiectasia 2: A clue to its pathogenesis

Indian Journal of Ophthalmology, 2015
Macular telangiectasia type 2 also known as idiopathic perifoveal telangiectasia and juxtafoveolar retinal telangiectasis type 2A is an acquired bilateral neurodegenerative macular disease that manifests itself during the fifth or sixth decades of life ...
Lihteh Wu
doaj   +1 more source

SUBFOVEAL NODULE IN COATS' DISEASE: Toward an Updated Classification Predicting Visual Prognosis. [PDF]

, 2017
To determine the prevalence, clinical characteristics and nature of subfoveal nodules in Coats' disease and the associated impact on the long-term visual outcome.
Daruich, A.L., Matet, A., Moulin, A.P., Munier, F.L., Tran, H.V.   +4 more
core   +1 more source

A Rare Case Of Unilateral Adult Onset Coats’ Disease

Delhi Journal of Ophthalmology, 2018
Coats’ disease is typically seen in childhood and less commonly among adults. The Adult onset form is manifested by various findings typical of Coats’ disease which include the unilateral nature of the disease, male predominance, vascular telangiectasis,
Sonam Mahajan, Ohm Patel, Rahul Sharma, Vivek Kumar   +3 more
doaj   +1 more source

Levels of cytokines in the aqueous humor guided treatment of refractory macular edema in adult-onset coats’ disease

BMC Ophthalmology, 2020
Background Two cases with refractory macular edema secondary to adult-onset Coats’ disease underwent unsatisfactory treatment by intravitreal injections of anti-vascular endothelial growth factor (VEGF) drugs and retinal photocoagulation.
Yewei Wang, Hua Fan, Ke Gao, Wei He, Yong Tao   +4 more
doaj   +1 more source

Outer retinal circular structures in patients with Bietti crystalline retinopathy. [PDF]

, 2011
[Background] : Bietti crystalline retinopathy (BCR) is a distinct retinal degenerative disease characterised by retinal degeneration with many yellow–white crystals located mainly at the posterior pole area.
Guo, Congrong, Kojima, Hiroshi, Kurimoto, Masafumi, Makiyama, Yukiko, Nakagawa, Satoko, Ogino, Ken, Otani, Atsushi, Yoshimura, Nagahisa   +7 more
core   +1 more source

A rare case of occlusive juxtafoveolar retinal telangiectasias associated with lesions of the central nervous system: A cerebroretinal vasculopathy like phenotype without mutations in the TREX1 gene

American Journal of Ophthalmology Case Reports, 2020
Purpose: To report a rare case of bilateral occlusive juxtafoveolar retinal telangiectasias associated with central nervous system lesions and renal impairment.
Mark P. Seraly, Karim H. Badawi, Sumeet K. Gupta, Nabil M. Jabbour, Brian Ellis, Monique Leys   +5 more
doaj   +1 more source

Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data [PDF]

, 2017
Infantile or early onset is estimated to occur in around 10% of all facioscapulohumeral dystrophy (FSHD) patients. Although small series of early onset FSHD patients have been reported, comprehensive data on the clinical phenotype is missing.
Brouwer, Oebele F., Dorobek, Malgorzata, Erasmus, Corrie E., Goselink, Rianne J. M., Mah, Jean K., Nikolic, Ana, Okkersen, Kees, Padberg, George W., Schreuder, Tim H. A., Tupler, Rossella, Van Engelen, Baziel G. M., Voermans, Nicol C.   +11 more
core   +2 more sources