Literature DB >> 20564735

Developmental and benign movement disorders in childhood.

Cecilia Bonnet1, Agathe Roubertie, Diane Doummar, Nadia Bahi-Buisson, Valérie Cochen de Cock, Emmanuel Roze.   

Abstract

Developmental and benign movement disorders are a group of movement disorders with onset in the neonatal period, infancy, or childhood. They are characterized by the absence of associated neurological manifestations and by their favorable outcome, although developmental abnormalities can be occasionally observed. Knowledge of the clinical, neurophysiological, and pathogenetic aspects of these disorders is poor. Based on a comprehensive review of the literature and our practical experience, this article summarizes current knowledge in this area. We pay special attention to the recognition and management of these movement disorders in children. (c) 2010 Movement Disorder Society.

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Year:  2010        PMID: 20564735     DOI: 10.1002/mds.22944

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  17 in total

Review 1.  Congenital mirror movements: a clue to understanding bimanual motor control.

Authors:  Cécile Galléa; Traian Popa; Ségolène Billot; Aurélie Méneret; Christel Depienne; Emmanuel Roze
Journal:  J Neurol       Date:  2011-06-03       Impact factor: 4.849

2.  RAD51 haploinsufficiency causes congenital mirror movements in humans.

Authors:  Christel Depienne; Delphine Bouteiller; Aurélie Méneret; Ségolène Billot; Sergiu Groppa; Stephan Klebe; Fanny Charbonnier-Beaupel; Jean-Christophe Corvol; Jean-Paul Saraiva; Norbert Brueggemann; Kailash Bhatia; Massimo Cincotta; Vanessa Brochard; Constance Flamand-Roze; Wassila Carpentier; Sabine Meunier; Yannick Marie; Marion Gaussen; Giovanni Stevanin; Rosine Wehrle; Marie Vidailhet; Christine Klein; Isabelle Dusart; Alexis Brice; Emmanuel Roze
Journal:  Am J Hum Genet       Date:  2012-02-02       Impact factor: 11.025

Review 3.  Pediatric migraine variants: a review of epidemiology, diagnosis, treatment, and outcome.

Authors:  Ana Marissa Lagman-Bartolome; Christine Lay
Journal:  Curr Neurol Neurosci Rep       Date:  2015-06       Impact factor: 5.081

4.  Congenital mirror movements: no mutation in DNAL4 in 17 index cases.

Authors:  Aurélie Méneret; Oriane Trouillard; Marie Vidailhet; Christel Depienne; Emmanuel Roze
Journal:  J Neurol       Date:  2014-09-19       Impact factor: 4.849

5.  Reply: Congenital mirror movements: lack of decussation of pyramids Mirror movement: from physiopathology to treatment perspectives.

Authors:  Cecile Gallea; Traian Popa; Sabine Meunier; Emmanuel Roze
Journal:  Brain       Date:  2014-04-10       Impact factor: 13.501

6.  Mutations in the netrin-1 gene cause congenital mirror movements.

Authors:  Aurélie Méneret; Elizabeth A Franz; Oriane Trouillard; Thomas C Oliver; Yvrick Zagar; Stephen P Robertson; Quentin Welniarz; R J MacKinlay Gardner; Cécile Gallea; Myriam Srour; Christel Depienne; Christine L Jasoni; Caroline Dubacq; Florence Riant; Jean-Charles Lamy; Marie-Pierre Morel; Raphael Guérois; Jessica Andreani; Coralie Fouquet; Mohamed Doulazmi; Marie Vidailhet; Guy A Rouleau; Alexis Brice; Alain Chédotal; Isabelle Dusart; Emmanuel Roze; David Markie
Journal:  J Clin Invest       Date:  2017-09-25       Impact factor: 14.808

7.  Gómez-López-Hernández syndrome: reappraisal of the diagnostic criteria.

Authors:  Biayna Sukhudyan; Varsine Jaladyan; Gayane Melikyan; Jan Ulrich Schlump; Eugen Boltshauser; Andrea Poretti
Journal:  Eur J Pediatr       Date:  2010-07-23       Impact factor: 3.183

8.  Gomez-Lopez-Hernández syndrome: First reported case from the Indian subcontinent.

Authors:  Anita Choudhary; Priyanka Minocha; Sadasivan Sitaraman
Journal:  Intractable Rare Dis Res       Date:  2017-02

9.  Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

Authors:  Aurélie Méneret; Christel Depienne; Florence Riant; Oriane Trouillard; Delphine Bouteiller; Massimo Cincotta; Pierre Bitoun; Julia Wickert; Isabelle Lagroua; Ana Westenberger; Alessandra Borgheresi; Diane Doummar; Marcello Romano; Simone Rossi; Luc Defebvre; Linda De Meirleir; Alberto J Espay; Simona Fiori; Stephan Klebe; Chloé Quélin; Sabine Rudnik-Schöneborn; Ghislaine Plessis; Russell C Dale; Susan Sklower Brooks; Karolina Dziezyc; Pierre Pollak; Jean-Louis Golmard; Marie Vidailhet; Alexis Brice; Emmanuel Roze
Journal:  Neurology       Date:  2014-05-07       Impact factor: 9.910

10.  Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder.

Authors:  Iltaf Ahmed; Kirti Mittal; Taimoor I Sheikh; Nasim Vasli; Muhammad Arshad Rafiq; Anna Mikhailov; Mehrnaz Ohadi; Huda Mahmood; Guy A Rouleau; Attya Bhatti; Muhammad Ayub; Myriam Srour; Peter John; John B Vincent
Journal:  Hum Genet       Date:  2014-08-07       Impact factor: 4.132

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