Literature DB >> 2189924

Ocular anomalies in fragile X syndrome.

D M Maino1, D Schlange, J H Maino, B Caden.   

Abstract

Fragile X (fra[X]) syndrome is a newly discovered, but relatively common, genetic disorder with an estimated frequency of 1:1000. Several ocular dysfunctions may be associated with this syndrome, but there are few articles that fully report on these. A review of this genetic disorder is provided, as well as a discussion of a case review of a family with three siblings with fragile X syndrome. Since this disorder is the most common familial cause of mental retardation, is second only to Down's syndrome as a genetic cause for mental retardation, and may play a significant role in learning disabilities, the eye care practitioner should be aware of its importance.

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Mesh:

Year:  1990        PMID: 2189924

Source DB:  PubMed          Journal:  J Am Optom Assoc        ISSN: 0003-0244


  3 in total

Review 1.  Fragile X syndrome. Molecular and clinical insights and treatment issues.

Authors:  R J Hagerman
Journal:  West J Med       Date:  1997-02

Review 2.  Fragile X syndrome: A review of clinical management.

Authors:  Reymundo Lozano; Atoosa Azarang; Tanaporn Wilaisakditipakorn; Randi J Hagerman
Journal:  Intractable Rare Dis Res       Date:  2016-08

3.  Evaluation of MFRP as a candidate gene for high hyperopia.

Authors:  Panfeng Wang; Zhikuan Yang; Shiqiang Li; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
Journal:  Mol Vis       Date:  2009-01-23       Impact factor: 2.367

  3 in total

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