R102W mutation in the RS1 gene responsible for retinoschisis and recurrent glaucoma  

作　　者：Xiu-Feng Huang Chang-Sen Tu Dong-Jun Xing De-Kang Gan Ge-Zhi Xu Zi-Bing Jin 

机构地区：[1]Division of Ophthalmic Genetics,Laboratory for Stem Cell & Retinal Regeneration,the Eye Hospital of Wenzhou Medical University [2]The State Key Laboratory Cultivation Base and NHFPC Key Laboratory of Vision Science [3]Department of Ophthalmology,the EENT Hospital of Fudan University

出　　处：《International Journal of Ophthalmology(English edition)》2014年第1期169-172,共4页国际眼科杂志（英文版）

基　　金：Supported by the National Key Basic Research Program(2013CB967502,2013CB967503);Most Major Projects(2012YQ12008004);Qianjiang Talents Project(2012R10072);Zhejiang Provincial Natural Science Foundation of China(No.LR13H120001)

摘　　要：AIM: To identify the mutations in RS1 gene associated with typical phenotype of X-linked juvenile retinoschisis(XLRS) and a rare condition of concomitant glaucoma. ·METHODS: Complete ophthalmic examinations were performed in the proband. The coding regions of the RS1 gene that encode retinoschisin were amplified by polymerase chain reaction and directly sequenced. ·RESULTS: The proband showed a typical phenotype of XLRS with large peripheral retinal schisis in both eyes,involving the macula and combined with foveal cystic change,reducing visual acuity. A typical phenotype of recurrent glaucoma with high intraocular pressure(IOP) and reduced visual field was also demonstrated with the patient. Mutation analysis of RS1 gene revealed R102W(c.304C】T) mutations in the affected male,and his mother was proved to be a carrier with the causative mutation and another synonymous polymorphism(c.576C】CT). ·CONCLUSION: We identified the genetic variations of a Chinese family with typical phenotype of XLRS and glaucoma. The severe XLRS phenotypes associated with R102W mutations reveal that the mutation determines a notable alteration in the function of the retinoschisin protein. Identification of the disease-causing mutation is beneficial for future clinical references.AIM: To identify the mutations in RS1 gene associated with typical phenotype of X-linked juvenile retinoschisis(XLRS) and a rare condition of concomitant glaucoma. ·METHODS: Complete ophthalmic examinations were performed in the proband. The coding regions of the RS1 gene that encode retinoschisin were amplified by polymerase chain reaction and directly sequenced. ·RESULTS: The proband showed a typical phenotype of XLRS with large peripheral retinal schisis in both eyes,involving the macula and combined with foveal cystic change,reducing visual acuity. A typical phenotype of recurrent glaucoma with high intraocular pressure(IOP) and reduced visual field was also demonstrated with the patient. Mutation analysis of RS1 gene revealed R102W(c.304C>T) mutations in the affected male,and his mother was proved to be a carrier with the causative mutation and another synonymous polymorphism(c.576C>CT). ·CONCLUSION: We identified the genetic variations of a Chinese family with typical phenotype of XLRS and glaucoma. The severe XLRS phenotypes associated with R102W mutations reveal that the mutation determines a notable alteration in the function of the retinoschisin protein. Identification of the disease-causing mutation is beneficial for future clinical references.

关 键 词：X-linked retinoschisis GLAUCOMA RS1 gene MUTATION 

分 类 号：R775[医药卫生—眼科]