Literature DB >> 18054699

Muscle pain as the only presenting symptom in a girl with dystrophinopathy.

Berten P Ceulemans1, Katrien Storm, Edwin Reyniers, Luc Callewaert, Jean Jacques Martin.   

Abstract

We present a family with dystrophinopathy in whom the proband is a female aged 4.5 years, who presented with exertional muscle pain without weakness. Familial analysis identified a maternal nephew of the proband who demonstrated a similar clinical picture, with asymptomatic cardiomyopathy. A DNA analysis revealed an in-frame deletion in the proximal part of domain II of the dystrophin gene. Extensive familial analysis indicated that the asymptomatic maternal grandfather transmitted the deletion. This is the first report of a young female patient with exertional muscle pain as the only early presenting symptom of dystrophinopathy.

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Year:  2008        PMID: 18054699     DOI: 10.1016/j.pediatrneurol.2007.09.006

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  7 in total

1.  Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age.

Authors:  Sandra Mercier; Annick Toutain; Aurélie Toussaint; Martine Raynaud; Claire de Barace; Pascale Marcorelles; Laurent Pasquier; Martine Blayau; Caroline Espil; Philippe Parent; Hubert Journel; Leila Lazaro; Jon Andoni Urtizberea; Alexandre Moerman; Laurence Faivre; Bruno Eymard; Kim Maincent; Romain Gherardi; Denys Chaigne; Rabah Ben Yaou; France Leturcq; Jamel Chelly; Isabelle Desguerre
Journal:  Eur J Hum Genet       Date:  2013-01-09       Impact factor: 4.246

2.  Three cases of manifesting female carriers in patients with Duchenne muscular dystrophy.

Authors:  Tae-Jin Song; Kyung-A Lee; Seong-Woong Kang; Hanna Cho; Young-Chul Choi
Journal:  Yonsei Med J       Date:  2011-01       Impact factor: 2.759

3.  Pseudometabolic presentation of dystrophinopathy due to a missense mutation.

Authors:  Aravindhan Veerapandiyan; Vandana Shashi; Yong-Hui Jiang; William Brian Gallentine; Kelly Schoch; Edward Clinton Smith
Journal:  Muscle Nerve       Date:  2010-12       Impact factor: 3.217

Review 4.  Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy.

Authors:  Emanuela Viggiano; Manuela Ergoli; Esther Picillo; Luisa Politano
Journal:  Hum Genet       Date:  2016-04-21       Impact factor: 4.132

5.  MRI/MRS evaluation of a female carrier of Duchenne muscular dystrophy.

Authors:  Sean C Forbes; Donovan J Lott; Richard S Finkel; Claudia Senesac; Barry J Byrne; H Lee Sweeney; Glenn A Walter; Krista Vandenborne
Journal:  Neuromuscul Disord       Date:  2012-10-01       Impact factor: 4.296

6.  Mitochondrial Dysfunction Is an Early Consequence of Partial or Complete Dystrophin Loss in mdx Mice.

Authors:  Timothy M Moore; Amanda J Lin; Alexander R Strumwasser; Kevin Cory; Kate Whitney; Theodore Ho; Timothy Ho; Joseph L Lee; Daniel H Rucker; Christina Q Nguyen; Aidan Yackly; Sushil K Mahata; Jonathan Wanagat; Linsey Stiles; Lorraine P Turcotte; Rachelle H Crosbie; Zhenqi Zhou
Journal:  Front Physiol       Date:  2020-06-19       Impact factor: 4.566

7.  The lncRNA H19 alleviates muscular dystrophy by stabilizing dystrophin.

Authors:  Yaohua Zhang; Yajuan Li; Qingsong Hu; Yutao Xi; Zhen Xing; Zhao Zhang; Lisa Huang; Jianbo Wu; Ke Liang; Tina K Nguyen; Sergey D Egranov; Chengcao Sun; Zilong Zhao; David H Hawke; Jin Li; Deqiang Sun; Jean J Kim; Ping Zhang; Jie Cheng; Abid Farida; Mien-Chie Hung; Leng Han; Radbod Darabi; Chunru Lin; Liuqing Yang
Journal:  Nat Cell Biol       Date:  2020-10-26       Impact factor: 28.213

  7 in total

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