IJRTIdiopathic Juxtafoveal Retinal Telangiectasis
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This condition, named by Yannuzzi et al., (1) refers to idiopathic juxtaretinal telangiectasia (IJRT) type 2A according to the classification system introduced by Gass and Blodi (2) in 1993.
It was first described by Gass and Oyakawa [1] and Gass and Blodi [2] and named idiopathic juxtafoveolar retinal telangiectasis (IJRT).
IJRT encompasses a group of disorders characterised by retinal telangiectasias, superficial retinal crystalline deposits, right-angle venules and intra-retinal pigment plaques (Figure 8).