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Ophthalmic Genetics Volume 28, 2007 - Issue 4
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Review

A Review of the Molecular Genetics of Congenital Idiopathic Nystagmus (CIN)

James Self Clinical Neurosciences Division, University of Southampton, Southampton, United Kingdom; Southampton Eye Unit, Southampton General Hospital, Southampton, United Kingdom
&
Andrew Lotery Clinical Neurosciences Division, University of Southampton, Southampton, United Kingdom; Southampton Eye Unit, Southampton General Hospital, Southampton, United Kingdom
Pages 187-191 | Received 12 Jul 2007, Accepted 27 Aug 2007, Published online: 08 Jul 2009

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Michael C. Brodsky. (2020) Congenital Nystagmus and Its Congeners. Journal of Binocular Vision and Ocular Motility 70:2, pages 63-70.
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Vincent Michaud, Sabine Defoort-Dhellemmes, Isabelle Drumare, Perrine Pennamen, Claudio Plaisant, Eulalie Lasseaux & Benoit Arveiler. (2019) Clinical and molecular findings of FRMD7 related congenital nystagmus as adifferential diagnosis of ocular albinism. Ophthalmic Genetics 40:2, pages 161-164.
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Asma AA Zahidi, J Margaret Woodhouse, Jonathan T Erichsen & Matt J Dunn. (2017) Infantile nystagmus: an optometrist’s perspective. Clinical Optometry 9, pages 123-131.
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Morgan Bertsch, Michael Floyd, Taylor Kehoe, Wanda Pfeifer & Arlene V. Drack. (2017) The clinical evaluation of infantile nystagmus: What to do first and why. Ophthalmic Genetics 38:1, pages 22-33.
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Doreen Huppert, Michael Strupp, Harald Mückter & Thomas Brandt. (2011) Which medication do I need to manage dizzy patients?. Acta Oto-Laryngologica 131:3, pages 228-241.
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. (2010) Abstracts of the 2010 Meeting of the International Neuro-Ophthalmology Society, Lyon, France. Neuro-Ophthalmology 34:3, pages 131-288.
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Articles from other publishers (27)

Lei Jiang, Yulei Li, Kangjuan Yang, Yuping Wang, Jiuxiang Wang, Xiaoniu Cui, Jinglin Mao, Yong Gao, Ping Yi, Lejin Wang & Jing Yu Liu. (2020) FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus Syndrome. Investigative Opthalmology & Visual Science 61:5, pages 41.
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Alma Kurent, Jelka Brecelj & Branka Stirn-Kranjc. (2018) Electroretinograms in idiopathic infantile nystagmus, optic nerve hypoplasia and albinism. European Journal of Ophthalmology 30:1, pages 147-154.
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Shan Wu, Sheng Deng, Zhi Song, Hongbo Xu, Zhijian Yang, Xin Liu, Li Qi, Hao Deng & Lamei Yuan. (2019) A Disease-Causing FRMD7 Variant in a Chinese Family with Infantile Nystagmus. Journal of Molecular Neuroscience 67:3, pages 418-423.
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N. Gravier. (2018) Le bilan étiologique d’un nystagmus chez l’enfant. Journal Français d'Ophtalmologie 41:9, pages 868-878.
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Y‐C. Huang, S‐Y. Hsu & Y‐H. Young. (2018) Comorbid inner ear disorders in 50 patients with congenital nystagmus. Clinical Otolaryngology 43:4, pages 1171-1177.
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Jae-Hwan Choi, Jae-Ho Jung, Eun Hye Oh, Jin-Hong Shin, Hyang-Sook Kim, Je Hyun Seo, Seo Young Choi, Min-Ji Kim, Hee Young Choi, Changwook Lee & Kwang-Dong Choi. (2018) Genotype and Phenotype Spectrum of FRMD7 -Associated Infantile Nystagmus Syndrome . Investigative Opthalmology & Visual Science 59:7, pages 3181.
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Michael C. BrodskyMichael C. Brodsky. 2016. Pediatric Neuro-Ophthalmology. Pediatric Neuro-Ophthalmology 495 567 .
Ping Yu, Yun Cui, Wanshi Cai, Honghu Wu, Xiaoqiang Xiao, Qianzhi Shao, Liang Ma, Sen Guo, Nana Wu, Zi-Bing Jin, Yongjin Wang, Tao Cai, Zhong Sheng Sun & Jia Qu. (2015) Lysosomal storage disease in the brain: mutations of the β-mannosidase gene identified in autosomal dominant nystagmus. Genetics in Medicine 17:12, pages 971-979.
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Michael D. Richards & Agnes Wong. (2015) Infantile nystagmus syndrome: clinical characteristics, current theories of pathogenesis, diagnosis, and management. Canadian Journal of Ophthalmology 50:6, pages 400-408.
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Michael Strupp & Thomas Brandt. 2015. Evidence‐Based Neurology: Management of Neurological Disorders. Evidence‐Based Neurology: Management of Neurological Disorders 279 290 .
Brandon C. Gabel, Michael L. Levy & John R. Crawford. (2015) Delayed Diagnosis of Enhancing Posterior Fossa Tumors Mimicking the Tela Choroidea of the Fourth Ventricle. World Neurosurgery 84:3, pages 865.e1-865.e5.
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Jay E. Self, Ahmed Salman & Marion F. Hedley-Lewis. (2015) Is This Actually CIN?. Pediatric Neurology 53:3, pages e11.
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Sarita B. Dave & Patrick J. M. Lavin. 2014. Neurologic Differential Diagnosis. Neurologic Differential Diagnosis 287 298 .
. 2014. Neurologic Differential Diagnosis. Neurologic Differential Diagnosis 1 546 .
J Chhetri, G Jacobson & N Gueven. (2014) Zebrafish—on the move towards ophthalmological research. Eye 28:4, pages 367-380.
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Yi Guo, Zhi Song, Hongbo Xu, Junhui Yi, Wen Zheng, Hong Xiang, Xiong Deng, Hongwei Lv, Kai Gao, Yong Qi & Hao Deng. (2014) Heterogeneous phenotype in a family with the FERM domain-containing 7 gene R335X mutation. Canadian Journal of Ophthalmology 49:1, pages 50-53.
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Claudia Jandeck, Klaus Rüther & Elisabeth Schulz. 2014. Neuropädiatrie. Neuropädiatrie 417 448 .
Lin Li, Xueshan Xiao, Changxian Yi, Xiaodong Jiao, Xiangming Guo, James Fielding Hejtmancik & Qingjiong Zhang. (2012) Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3–q32.1. Journal of Human Genetics 57:12, pages 756-759.
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N. Gravier. (2012) Bilan d’un nystagmus. EMC - Ophtalmologie 9:1, pages 1-7.
Crossref
Patrick J.M. Lavin. 2012. Neurology in Clinical Practice. Neurology in Clinical Practice 587 633 .
Colette M. Maurer, Ying-Yu Huang & Stephan C.F. Neuhauss. (2011) Application of zebrafish oculomotor behavior to model human disorders. revneuro 22:1, pages 5-16.
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Cecilia Bonnet, Agathe Roubertie, Diane Doummar, Nadia Bahi‐Buisson, Valérie Cochen de Cock & Emmanuel Roze. (2010) Developmental and benign movement disorders in childhood. Movement Disorders 25:10, pages 1317-1334.
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Michael C. BrodskyMichael C. Brodsky. 2010. Pediatric Neuro-Ophthalmology. Pediatric Neuro-Ophthalmology 383 441 .
Eric R. Eggenberger. (2009) NYSTAGMUS AND OTHER ABNORMAL EYE MOVEMENTS. CONTINUUM: Lifelong Learning in Neurology 15, pages 200-212.
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Michael Strupp & Thomas Brandt. (2009) Review: Current treatment of vestibular, ocular motor disorders and nystagmus. Therapeutic Advances in Neurological Disorders 2:4, pages 223-239.
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. 2009. Neurologische Therapie im Kindesalter. Neurologische Therapie im Kindesalter 347 372 .
Xiang HeFeng GuZe WangChong WangYi TongYujing WangJuhua YangWei LiuMeng ZhangXu Ma. (2008) A Novel Frameshift Mutation in FRMD7 Causing X-Linked Idiopathic Congenital Nystagmus . Genetic Testing 12:4, pages 607-613.
Crossref

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