Literature DB >> 12525540

Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.

N K Ragge1, C Hartley, A M Dearlove, J Walker, I Russell-Eggitt, C M Harris.   

Abstract

PURPOSE: To determine a gene locus for a family with a dominantly inherited vestibulocerebellar disorder characterised by early onset, but not congenital nystagmus.
DESIGN: Observational and experimental study.
METHODS: We carried out a phenotypic study of a unique four generation family with nystagmus. We performed genetic linkage studies including a genome wide search.
RESULTS: Affected family members developed vestibulocerebellar type nystagmus in the first two years of life. A higher incidence of strabismus was noted in affected members. Haplotype construction and analysis of recombination events linked the disorder to a locus (NYS4) on chromosome 13q31-q33 with a lod score of 6.322 at theta=0 for D13S159 and narrowed the region to a 13.8 cM region between markers D13S1300 and D13S158.
CONCLUSIONS: This study suggests that the early onset acquired nystagmus seen in this family is caused by a single gene defect. Identification of the gene may hold the key to understanding pathways for early eye stabilisation and strabismus.

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Year:  2003        PMID: 12525540      PMCID: PMC1735258          DOI: 10.1136/jmg.40.1.37

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  10 in total

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4.  Recreational concentrations of alcohol enhance synaptic inhibition of cerebellar unipolar brush cells via pre- and postsynaptic mechanisms.

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5.  The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.

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6.  Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation.

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7.  Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation.

Authors:  Shery Thomas; Mervyn G Thomas; Caroline Andrews; Wai-Man Chan; Frank A Proudlock; Rebecca J McLean; Archana Pradeep; Elizabeth C Engle; Irene Gottlob
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8.  Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus.

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9.  A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family.

Authors:  Xiang He; Feng Gu; Yujing Wang; Jinting Yan; Meng Zhang; Shangzhi Huang; Xu Ma
Journal:  Mol Vis       Date:  2008-01-11       Impact factor: 2.367

10.  Five novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmus.

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  10 in total

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