Results 101 to 110 of about 2,508,923 (191)
Hematological and atherogenic indices in patients with exfoliation syndrome and exfoliation glaucoma
B. Erdem, M. Gok
semanticscholar +1 more source
Increasing pathophysiologic evidence indicates that exfoliation syndrome, a systemic process involving various visceral organs, frequently manifests itself first in the eyes as exfoliation of the lens and glaucoma. Exfoliation syndrome occurs when several tissues synthesize an abnormal basement membrane protein. This protein may obstruct the trabecular
Y J, Lin, T H, Wang, S C, Kao, P T, Hung
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Capsular Glaucoma and Other Ophthalmic Complications of Pseudoexfoliation Syndrome
Pseudoexfoliation syndrome is an age-related disorder of the extracellular matrix, characterized by the deposition of pathological fibrillar material in the structures of the anterior segment of the eye and in extraocular tissues.
Piotr Witold Stępień +5 more
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Papillon-Lefevre syndrome: A case report
Papillon-Lefevre syndrome is a rare autosomal recessive genetic disorder. The clinical manifestations include palmer planter hyperkeratosis with precocious progressive periodontal disease that results in premature exfoliation of primary and permanent ...
Subramaniam P, Mathew S, Gupta K
doaj
Objective To summarize and analyze the skin care methods for and outcomes of patients with Stevens-Johnson syndrome (SJS) or toxic epidermal necrolysis (TEN).
HE Xueyu +6 more
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Coexistence of MRCS syndrome, extremely long axis and exfoliation syndrome: a case report and literature review. [PDF]
Wang X, Jiang X, Liu Z, Wang C, Li X.
europepmc +1 more source
剥脱综合征性青光眼(peseudo exfoliation glaucoma,PEG)也称剥脱性青光眼,是继发于剥脱综合征(exfoliation syndrome,ES)的一种青光眼类型。扩瞳后可见晶状体前囊表面沉着物的3个区[1-3]。本病无明显病因[4-9],多无自觉症状,发病时已出现明显视功能损害,目前疗效较差。现将我院2006年1月 ...
李丹, 李弘, 胥利平, 李秀昆
doaj
Deborah KL Tan,1 Tin Aung,1–3 Shamira A Perera1,21Singapore National Eye Centre, Singapore; 2Singapore Eye Research Institute, Singapore; 3National University of Singapore, Yong Loo Lin School of Medicine, SingaporeBackground: Delamination of ...
Tan DKL, Aung T, Perera SA
doaj
Alexios A Panoutsopoulos,1 Vassiliki S Gartaganis,2 Marios P Giannakopoulos,1 Panos D Goumas,3 Evangelos D Anastassiou,4 Sotirios P Gartaganis1 1Department of Ophthalmology, School of Medicine, University of Patras, Achaia, Greece; 2Protein ...
Panoutsopoulos AA +5 more
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MSX1 Mutation in Witkop Syndrome; A Case Report
The Witkop syndrome is a rare autosomal dominant disorder characterized by the absence of several teeth and abnormalities of the nails. This is the first report of a rare genetic tooth and nail syndrome diagnosed in a 2.5-year-old boy with early ...
Faezeh Ghaderi +3 more
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