Literature DB >> 8240694

Unusual fetal movement in congenital myotonic dystrophy.

C D Hsu1, T I Feng, T O Crawford, T R Johnson.   

Abstract

Congenital myotonic dystrophy is the most extreme and early expression of a multisystem autosomal dominant disorder. Decreased fetal and infantile movement is a defining feature. We report a case of congenital myotonic dystrophy with an unusual pattern of persistent repetitive fetal movements detected by a Doppler fetal movement detector.

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Year:  1993        PMID： 8240694     DOI： 10.1159/000263825

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN： 1015-3837            Impact factor:   2.587


  2 in total

1.  CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.

Authors:  Lise Barbé; Stella Lanni; Arturo López-Castel; Silvie Franck; Claudia Spits; Kathelijn Keymolen; Sara Seneca; Stephanie Tomé; Ioana Miron; Julie Letourneau; Minggao Liang; Sanaa Choufani; Rosanna Weksberg; Michael D Wilson; Zdenek Sedlacek; Cynthia Gagnon; Zuzana Musova; David Chitayat; Patrick Shannon; Jean Mathieu; Karen Sermon; Christopher E Pearson
Journal:  Am J Hum Genet       Date:  2017-03-02       Impact factor: 11.025

2.  Women's and clinicians perspectives of presentation with reduced fetal movements: a qualitative study.

Authors:  R M D Smyth; W Taylor; A E Heazell; C Furber; M Whitworth; T Lavender
Journal:  BMC Pregnancy Childbirth       Date:  2016-09-26       Impact factor: 3.007
  2 in total

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