Idiopathic Juxtafoveolar Retinal Telangiectasis: Update of.
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.
It was first classified as idiopathic juxtafoveal retinal telangiectasis and subsequently was subdivided into type 1 (aneurysmal telangiectasia) and type 2 (perifoveal telangiectasia-nonproliferative or proliferative) (1, 2). Type 1 IMT is almost always unilateral and occurs predominantly in middle-aged men. It is characterised by retinal telangiectasia that is commonly confined to the.
Idiopathic Perifoveal Telangiectasis is commonly referred to as macular telangiectasia, a retinal disorder that affects the center most part of the macula. This poorly understood disease is most common in people between 40 to 60 years old.
Idiopathic Macular Telangiectasia type 2 (IMT2) is an acquired,. termed idiopathic juxtafoveal retinal telangiectasis (4). In 1993, Gass and Blodi performed a meta-analysis examining 140 such cases over a 28-year period and refi ned the clinical spectrum of these entities with subgroups and stages. Th e resulting classifi cation structure resulted in 3 distinctive groups each with a.
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M acular telangiectasia Type 2 (MacTel2) is a bilateral, progressive retinal vascular disease that arises within the temporal, juxtafoveal region of the macula. 1, 2 Initially, the microvascular.
A simplified classification termed idiopathic macular telangiectasia with 2 distinct types (type I, or aneurysmal telangiectasia, and type II, or perifoveal telangiectasia) was proposed to produce.