Movement disorders in children: Recent advances in management

被引：0
作者：
Emilio Fernández-Alvarez
机构：
[1] Hospital Universitario Sant Joan de Déu,Neuropediatric Department
[2] Hospital universitario Sant Joan de Déu,Neuropediatric Department
来源：
The Indian Journal of Pediatrics | 2009年 / 76卷
关键词：
Pediatric movement disorders; Synthesis; Clinical observation; Advances; Management;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
In recent years there has been a growing interest towards pediatric movement disorders (PMD). The data derived from the synthesis of clinical observation, neuroimaging, biochemical and, molecular genetics studies have allowed for the identification of a significant number of pediatric diseases featuring movement disorders. The purpose of this review is to outline an approach to the advances in management of dystonia, neurotransmitter disorders, tics, and paroxysmal dyskinetic syndromes starting in children younger than 18 yr of age.
引用
收藏
页码：531 / 536
页数：5
相关论文
共 73 条
  • [1] Fernández-Alvarez E.(1998)Transient movements disorders in children J Neurol 245 1-5
  • [2] Dooley J.M.(2003)Fever-induced dystonia Pediatric Neurol 58 149-150
  • [3] Furey S.(2004)Toward a definition of childhood dystonia Curr Opin Pediatr 16 623-627
  • [4] Gordon K.E.(2008)DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA Lancet Neurol 7 215-222
  • [5] Wood E.P.(2008)Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families Mov Disord 23 28-34
  • [6] Sanger T.D.(2003)Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiency Neurology 60 335-337
  • [7] Camargos S.(2002)Tyrosine hydroxylase deficiency: clinical manifestations of catecholamine insufficiency in infancy Mov Disord 17 354-359
  • [8] Scholtz S.(2002)Mutations in Hum Molec Genet 11 971-978
  • [9] Simón-Sanchez J.(2005) gene are associated with benign hereditary chorea Neurology 64 1952-1954
  • [10] Paisán-Ruiz C.(1997)A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa Am J Hum Genet 61 889-898
12345678