Literature DB >> 27495203

Movement Disorders Presenting in Childhood.

Manju A Kurian, Russell C Dale.   

Abstract

PURPOSE OF REVIEW: This article provides an overview of movement disorders that present in childhood. Key clinical features are discussed, and a brief guide to management strategies is provided. Recent advances in the field of pediatric movement disorders are also a focus of the article. RECENT
FINDINGS: Advances in genetic technologies and cell biology have contributed greatly to the elucidation of underlying disease mechanisms in childhood movement disorders. This article discusses the expanding spectrum of both genetic and acquired movement disorders that present in childhood, including benign, acquired, genetic, and psychogenic movement disorders.
SUMMARY: Movement disorders in childhood comprise a wide spectrum of both genetic and acquired diseases, ranging from benign self-limiting conditions to more progressive phenotypes associated with significant morbidity and mortality. Elucidation of the underlying cause is achieved through accurate history, detailed clinical examination, review of video footage (including home videos), and, where appropriate, neuroimaging and laboratory investigations. Early accurate diagnosis will facilitate the instigation of appropriate management strategies.

Entities:  

Mesh:

Year:  2016        PMID: 27495203     DOI: 10.1212/CON.0000000000000367

Source DB:  PubMed          Journal:  Continuum (Minneap Minn)        ISSN: 1080-2371


  6 in total

1.  Recognizing the Common Origins of Dystonia and the Development of Human Movement: A Manifesto of Unmet Needs in Isolated Childhood Dystonias.

Authors:  Jean-Pierre Lin; Nardo Nardocci
Journal:  Front Neurol       Date:  2016-12-19       Impact factor: 4.003

2.  Vitamin-Responsive Movement Disorders in Children.

Authors:  Vishal Sondhi; Suvasini Sharma
Journal:  Ann Indian Acad Neurol       Date:  2020-06-05       Impact factor: 1.383

Review 3.  Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms.

Authors:  Lucia Abela; Manju A Kurian
Journal:  J Inherit Metab Dis       Date:  2018-06-13       Impact factor: 4.982

4.  Case report: discovery of 2 gene variants for aromatic L-amino acid decarboxylase deficiency in 2 African American siblings.

Authors:  Berrin Monteleone; Keith Hyland
Journal:  BMC Neurol       Date:  2020-01-09       Impact factor: 2.474

5.  Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases.

Authors:  Chiara Ticci; Daniele Orsucci; Anna Ardissone; Luca Bello; Enrico Bertini; Irene Bonato; Claudio Bruno; Valerio Carelli; Daria Diodato; Stefano Doccini; Maria Alice Donati; Claudia Dosi; Massimiliano Filosto; Chiara Fiorillo; Chiara La Morgia; Costanza Lamperti; Silvia Marchet; Diego Martinelli; Carlo Minetti; Maurizio Moggio; Tiziana Enrica Mongini; Vincenzo Montano; Isabella Moroni; Olimpia Musumeci; Elia Pancheri; Elena Pegoraro; Guido Primiano; Elena Procopio; Anna Rubegni; Roberta Scalise; Monica Sciacco; Serenella Servidei; Gabriele Siciliano; Costanza Simoncini; Deborah Tolomeo; Paola Tonin; Antonio Toscano; Flavia Tubili; Michelangelo Mancuso; Roberta Battini; Filippo Maria Santorelli
Journal:  J Clin Med       Date:  2021-05-12       Impact factor: 4.241

6.  Genetic landscape of pediatric movement disorders and management implications.

Authors:  Dawn Cordeiro; Garrett Bullivant; Komudi Siriwardena; Andrea Evans; Jeff Kobayashi; Ronald D Cohn; Saadet Mercimek-Andrews
Journal:  Neurol Genet       Date:  2018-09-26
  6 in total

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