Literature DB >> 26022459

Clinical and Genetic Characterization of Female Dystrophinopathy.

Seung Ha Lee1, Jung Hwan Lee1, Kyung A Lee2, Young Chul Choi3.   

Abstract

BACKGROUND AND
PURPOSE: Duchenne and Becker muscular dystrophies are the most common X-linked recessive muscular dystrophies. Dystrophin gene mutations usually affect men, but reportedly 2.5-7.8% of women are affected and are classified as symptomatic carriers. The aim of this study was to clinically and genetically characterize symptomatic female dystrophinopathy carriers.
METHODS: The clinical and genetic data of 11 female dystrophinopathy carriers among 285 patients who underwent multiplex ligation-dependent probe amplification (MLPA) analysis for the dystrophin gene were reviewed. Women with muscle weakness and/or dilated cardiomyopathy were classified as symptomatic carriers, while subjects with high serum creatine kinase (CK) levels and/or minor myopathic signs such as muscle cramps and myalgia were classified as asymptomatic.
RESULTS: Twelve female carriers were identified, but 1 symptomatic carrier who also had Turner syndrome was excluded from the study. Of the 11 included female carriers, 4 were symptomatic and 7 were asymptomatic. The age at symptom onset in the symptomatic female carriers ranged from 15 to 31 years (mean, 30.6 years), and the age at diagnosis for asymptomatic carriers ranged from 4 to 38 years (mean, 24.5 years). Serum CK levels were markedly elevated (mean, 1,301 IU/mL) in three of the four (75%) symptomatic female carriers, and mildly elevated in three of the seven (42%) asymptomatic female carriers. Symptomatic female carriers typically presented with asymmetric bilateral leg weakness as the initial symptom, with aggravated symptoms after labor.
CONCLUSIONS: Female dystrophinopathy is not uncommon, and it is an important factor with respect to males with dystrophinopathy who may be born to such patients. Screening with MLPA is useful because it can aid in early diagnosis and appropriate management.

Entities:  

Keywords:  dystrophinopathy; female; multiplex ligation-dependent probe amplification

Year:  2015        PMID: 26022459      PMCID: PMC4507379          DOI: 10.3988/jcn.2015.11.3.248

Source DB:  PubMed          Journal:  J Clin Neurol        ISSN: 1738-6586            Impact factor:   3.077


  21 in total

1.  Symptomatic dystrophinopathies in female children.

Authors:  Natashia Seemann; Kathy Selby; Laura McAdam; Doug Biggar; Hanna Kolski; Sharan Goobie; Grace Yoon; Craig Campbell
Journal:  Neuromuscul Disord       Date:  2010-12-24       Impact factor: 4.296

2.  Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

Authors:  J T Den Dunnen; P M Grootscholten; E Bakker; L A Blonden; H B Ginjaar; M C Wapenaar; H M van Paassen; C van Broeckhoven; P L Pearson; G J van Ommen
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

3.  Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study.

Authors:  E M Hoogerwaard; E Bakker; P F Ippel; J C Oosterwijk; D F Majoor-Krakauer; N J Leschot; A J Van Essen; H G Brunner; P A van der Wouw; A A Wilde; M de Visser
Journal:  Lancet       Date:  1999-06-19       Impact factor: 79.321

4.  Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy.

Authors:  E M Hoogerwaard; P A van der Wouw; A A Wilde; E Bakker; P F Ippel; J C Oosterwijk; D F Majoor-Krakauer; A J van Essen; N J Leschot; M de Visser
Journal:  Neuromuscul Disord       Date:  1999-07       Impact factor: 4.296

5.  Clinical investigation in Duchenne dystrophy: V. Use of creatine kinase and pyruvate kinase in carrier detection.

Authors:  R C Griggs; J R Mendell; M H Brooke; G M Fenichel; J P Miller; M Province; R T Moxley; D Huntzinger; A Vaughn; M Cohen
Journal:  Muscle Nerve       Date:  1985-01       Impact factor: 3.217

6.  A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales.

Authors:  A Norman; P Harper
Journal:  Clin Genet       Date:  1989-07       Impact factor: 4.438

7.  Muscle MRI in female carriers of dystrophinopathy.

Authors:  G Tasca; M Monforte; E Iannaccone; F Laschena; P Ottaviani; G Silvestri; M Masciullo; M Mirabella; S Servidei; E Ricci
Journal:  Eur J Neurol       Date:  2012-05-15       Impact factor: 6.089

8.  De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.

Authors:  J Chelly; F Marlhens; B Le Marec; M Jeanpierre; M Lambert; G Hamard; B Dutrillaux; J C Kaplan
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

9.  Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up.

Authors:  Francesca Magri; Alessandra Govoni; Maria Grazia D'Angelo; Roberto Del Bo; Serena Ghezzi; Gandossini Sandra; Anna Carla Turconi; Monica Sciacco; Patrizia Ciscato; Andreina Bordoni; Silvana Tedeschi; Francesco Fortunato; Valeria Lucchini; Sara Bonato; Costanza Lamperti; Domenico Coviello; Yvan Torrente; Stefania Corti; Maurizio Moggio; Nereo Bresolin; Giacomo Pietro Comi
Journal:  J Neurol       Date:  2011-03-12       Impact factor: 4.849

10.  Carrier woman of Duchenne muscular dystrophy mimicking inflammatory myositis.

Authors:  Jiyeol Yoon; Se Hoon Kim; Chang-Seok Ki; Min-Jung Kwon; Mie-Jin Lim; Seong-Ryul Kwon; Kowoon Joo; Chang-Gi Moon; Won Park
Journal:  J Korean Med Sci       Date:  2011-03-28       Impact factor: 2.153

View more
  8 in total

Review 1.  The importance of genetic diagnosis for Duchenne muscular dystrophy.

Authors:  Annemieke Aartsma-Rus; Ieke B Ginjaar; Kate Bushby
Journal:  J Med Genet       Date:  2016-01-11       Impact factor: 6.318

2.  Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan.

Authors:  Michio Kobayashi; Tomoyuki Hatakeyama; Masatoshi Ishizaki; Katsuhito Adachi; Mizuki Morita; Naohiro Yonemoto; Tsuyoshi Matsumura; Itaru Toyoshima; En Kimura
Journal:  Intern Med       Date:  2018-03-09       Impact factor: 1.271

3.  Clinical and genetic characteristics of female dystrophinopathy carriers.

Authors:  Jingzi Zhong; Yanshu Xie; Vidata Bhandari; Gang Chen; Yiwu Dang; Haixia Liao; Jiapeng Zhang; Dan Lan
Journal:  Mol Med Rep       Date:  2019-02-25       Impact factor: 2.952

4.  A Decade of Progress in Gene Targeted Therapeutic Strategies in Duchenne Muscular Dystrophy: A Systematic Review.

Authors:  Lam Chung Liang; Nadiah Sulaiman; Muhammad Dain Yazid
Journal:  Front Bioeng Biotechnol       Date:  2022-03-23

Review 5.  Advance genome editing technologies in the treatment of human diseases: CRISPR therapy (Review).

Authors:  Meryem Alagoz; Nasim Kherad
Journal:  Int J Mol Med       Date:  2020-05-19       Impact factor: 4.101

6.  Connexin-43 reduction prevents muscle defects in a mouse model of manifesting Duchenne muscular dystrophy female carriers.

Authors:  Julie Nouet; Eric Himelman; Kevin C Lahey; Qingshi Zhao; Diego Fraidenraich
Journal:  Sci Rep       Date:  2020-03-30       Impact factor: 4.379

7.  Population-Wide Duchenne Muscular Dystrophy Carrier Detection by CK and Molecular Testing.

Authors:  Shuai Han; Hong Xu; Jinxian Zheng; Junhui Sun; Xue Feng; Yue Wang; Wen Ye; Qing Ke; Yanwei Ren; Shulie Yao; Songying Zhang; Jianfen Chen; Robert C Griggs; Zhengyan Zhao; Ming Qi; Michele A Gatheridge
Journal:  Biomed Res Int       Date:  2020-09-27       Impact factor: 3.411

8.  Can symptomatic nmDuchenne carriers benefit from treatment with ataluren? Results of 193-month follow-up.

Authors:  Amir Dori; Michela Guglieri; Marianna Scutifero; Luigia Passamano; Antonio Trabacca; Luisa Politano
Journal:  Acta Myol       Date:  2021-12-31
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.