Dear Editor,We report the case of severe mixed-mechanism glaucoma observed in a monocular Axenfeld-Rieger syndrome(ARS) patient who was successfully managed with an ahmed glaucoma implant(AGI) followed by a novel tech...
Dear Editor,I am Dr.Satoru Kase,from the Department of Ophthalmology,Faculty of Medicine and Graduate School of Medicine,Hokkaido University.I write to present the case of clinicopathological findings in Axenfeld-Rieg...
BACKGROUND Axenfeld-Rieger syndrome(ARS)is an autosomal dominant genetic disease characterized by ocular developmental disorders and its association with torsion of wandering spleen(WS)has not been reported to date to...
Supported by China Postdoctoral Science Foundation Funded Project(No.2017M612211);the National Natural Science Foundation of China(No.81300742;No.81600721);the Shandong Province Medical and Health Technology Development Project(No.2016WS0265);the Science and Technology Plan of Qingdao(No.15-9-1-35-jch)
AIM: To describe a Chinese family affected by a severe form of Axenfeld-Rieger syndrome (ARS) and characterize the molecular defect in PITX2 in the family. METHODS: Patients presented with typical ARS from a Chin...
Project supported by the Qianjiang Talents Project of Zhejiang Province(No.2010R10067);the Zhejiang Key Innovation Team Project of China(No.2009R50039);the Zhejiang Key Laboratory Foundation of China(No.2011E10006)
Objective: Axenfeld-Rieger syndrome (ARS) is phenotypically and genetically heterogeneous. In this study we identified the underlying genetic defect in a Chinese family with ARS. Methods: A detailed family history...