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Telangiectasias, aside from presenting in many other conditions, are one of the features of the acronymically named CREST syndrome, a form of systemic scleroderma. The syndrome recognises the significantly co-presenting symptoms of calcinosis , Raynaud's phenomenon , esophageal dysmotility , sclerodactyly and telangiectasia.
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Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, [1] is a rare, neurodegenerative disease causing severe disability.
Unilateral nevoid telangiectasia is characterized by multiple chronic asymptomatic superficial blanching telangiectasias along dermatomes or Blaschko's lines, [3] with asymmetric skin involvement, [4] while symmetric instances have been infrequently recorded.
TEMPI syndrome is an orphan disease where the patients share five characteristics from which the acronym is derived: telangiectasias, elevated erythropoietin and erythrocytosis, monoclonal gammopathy, perinephric fluid collection, and intrapulmonary shunting.
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