Literature DB >> 20523356

Unique phenotype in a Chinese family pedigree: ectopia lentis with varicose great saphenous vein.

W Shen1, Q Fu, R Sui, J Wu, L Liu.   

Abstract

OBJECTIVE: To report a Chinese family affected with both ectopia lentis and varicose great saphenous vein.
DESIGN: Observational pedigree report. PARTICIPANTS: The family with a total of 53 members in five generations. In the kindred there were 16 affected adults (including 6 deceased), of which 7 were male and 9 were female. MAIN OUTCOME MEASURES: Patients in this family showed an autosomal dominant trait of ectopia lentis and varicose great saphenous vein, occurring in four successive generations. The onset ages for lens dislocation were between 38 and 52 years. No cardiovascular abnormality was observed. Four patients underwent intracapsular lens extraction surgery.
CONCLUSIONS: The phenotype of this family showed similarities with Marfan-related disorders. This is a unique phenotype of ectopia lentis with varicose great saphenous vein.

Entities:  

Mesh:

Year:  2010        PMID: 20523356     DOI: 10.1038/eye.2010.82

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN: 0950-222X            Impact factor:   3.775


  2 in total

1.  A possible genetic answer to a recently reported novel phenotype.

Authors:  K Khan; M Ali; C Inglehearn
Journal:  Eye (Lond)       Date:  2011-01-14       Impact factor: 3.775

2.  Novel mutation in FBN1 causes ectopia lentis and varicose great saphenous vein in one Chinese autosomal dominant family.

Authors:  Qing Fu; Peng Liu; Qingsheng Lu; Feng Wang; Hui Wang; Wei Shen; Fei Xu; Lin Liu; Yuri V Sergeev; Ruifang Sui
Journal:  Mol Vis       Date:  2014-06-12       Impact factor: 2.367

  2 in total

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