Literature DB >> 12868501

Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures.

A T J M Helderman-van den Enden1, H B Ginjaar, A L J Kneppers, E Bakker, M H Breuning, M de Visser.   

Abstract

We describe a patient with somatic mosaicism of a point mutation in the dystrophin gene causing benign muscular dystrophy with an unusual asymmetrical distribution of muscle weakness and contractures. To our knowledge this is the first patient with asymmetrical weakness and contractures in an ambulatory patient with a dystrophinopathy.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12868501     DOI: 10.1016/s0960-8966(02)00285-7

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  2 in total

1.  Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.

Authors:  Carl E G Bruder; Arkadiusz Piotrowski; Antoinet A C J Gijsbers; Robin Andersson; Stephen Erickson; Teresita Diaz de Ståhl; Uwe Menzel; Johanna Sandgren; Desiree von Tell; Andrzej Poplawski; Michael Crowley; Chiquito Crasto; E Christopher Partridge; Hemant Tiwari; David B Allison; Jan Komorowski; Gert-Jan B van Ommen; Dorret I Boomsma; Nancy L Pedersen; Johan T den Dunnen; Karin Wirdefeldt; Jan P Dumanski
Journal:  Am J Hum Genet       Date:  2008-02-14       Impact factor: 11.025

2.  Interplay between DMD point mutations and splicing signals in Dystrophinopathy phenotypes.

Authors:  Jonàs Juan-Mateu; Lidia González-Quereda; Maria José Rodríguez; Edgard Verdura; Kira Lázaro; Cristina Jou; Andrés Nascimento; Cecilia Jiménez-Mallebrera; Jaume Colomer; Soledad Monges; Fabiana Lubieniecki; Maria Eugenia Foncuberta; Samuel Ignacio Pascual-Pascual; Jesús Molano; Montserrat Baiget; Pia Gallano
Journal:  PLoS One       Date:  2013-03-25       Impact factor: 3.240

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.