Results 31 to 40 of about 8,263 (226)
Oral and periodontal manifestations associated with systemic sclerosis: A case series and review
Journal of Indian Society of Periodontology, 2012 Systemic sclerosis is a rare connective tissue disorder with a wide range of oral manifestations. This case series reports significant oral and periodontal changes and also makes an attempt to correlate oral and systemic findings in these patients which ...
Rekha Jagadish +2 more
doaj +1 more source
The Pan-American Journal of Ophthalmology, 2017 Purpose: To present a case of vaso-vagal syncope (VVS) after mydriatic eye drops in a patient with cutaneous hemangioma and intracerebral vascular abnormalities.
Sarah A Alowedi +3 more
doaj +3 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 +3 more
doaj +1 more source
Triple Therapy Management of Macular Telangiectasia
Delhi Journal of Ophthalmology, 2015 We report the case of a 65 year old lady presenting with sudden diminution of vision in her right eye (RE) with the best corrected visual acuity (BCVA) being counting fingers at 1 metre.
Hammad Rashid Nasti +3 more
doaj +1 more source
Glicose como causa e tratamento de necrose cutânea
Jornal Vascular BrasileiroResumo A escleroterapia continua sendo um dos procedimentos mais executados pelos cirurgiões vasculares brasileiros. O conhecimento das suas complicações é imprescindível para que possamos evitá-las.
Marcelo Luiz Brandão +2 more
doaj +1 more source
Newborn with cutis marmorata telangiectatica congenita: a case report and review of the literature
Pediatria PolskaCutis marmorata telangiectatica congenita (CMTC) is a rare vascular disorder characterized by persistent marbled erythema, vascular telangiectasia, and skin atrophy, with unknown etiology and prevalence. Associated congenital abnormalities occur in up to
Małgorzata Kamińska +5 more
doaj +1 more source
Telangiectasia retiniana parafoveal unilateral Unilateral parafoveal retinal telangiectasis
Revista 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 +1 more source
Anais Brasileiros de Dermatologia, 2014 The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions.
Juliana Catucci Boza +3 more
doaj +1 more source
Transcriptomics in Venous Leg Ulcers (VLU): A Systematic Review
Wound Repair and Regeneration, Volume 34, Issue 2, March/April 2026.ABSTRACT Venous leg ulcers (VLUs) are chronic wounds in the lower limbs that cause significant morbidity. The underlying biology underpinning non‐healing in VLUs is still poorly understood and differences in transcriptomic profiles may help elucidate biological pathways involved in wound chronicity.
Chien Lin Soh +3 more
wiley +1 more source
Uncommon skeletal findings in systemic sclerosis (scleroderma)
South African Journal of Radiology, 2002 Scleroderma or progressive systemic sclerosis is a diffuse disease characterised by excessive deposition of collagen and small-vessel arteritis. Systemic sclerosis is divided into two groups. 1.
Betsie van der Walt +2 more
doaj +1 more source