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Intrafamilial phenotype variation in Marfan syndrome ascertained by intragenic linkage analysis.

  • Ni Chung Lee*
  • , Betau Hwang
  • , Chia Hsiang Chen
  • , Dau Ming Niu
  • *此作品的通信作者
  • National Yang Ming Chiao Tung University

研究成果: 期刊稿件 › 文章 › 同行評審

3 引文 斯高帕斯(Scopus)

摘要

Marfan syndrome is an autosomal dominant fibrillinopathy caused by mutations of the fibrillin-1 (FBN1) gene. Although linkage analysis is often required to ascertain the disease status in family members, recombination is a problem. We analyzed 6 families including 18 patients using 4 intragenic microsatellite markers, located in intron 1, 5, 28, and 43, respectively, of the FBN1 gene. Haplotypes in all family members could be established, and segregation analysis showed no recombination between the markers and the disease. After confirming the diagnosis, intrafamilial analysis revealed clinical manifestations involving the ocular, cardiac, and skeletal systems. Intragenic linkage analysis in Marfan syndrome is very helpful in its diagnosis and management within affected families.

原文英語
頁(從 - 到)964-967
頁數4
期刊Journal of the Formosan Medical Association
卷104
發行號12
出版狀態已出版 - 12 2005
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