Literature DB >> 2388636

Rett syndrome and associated movement disorders.

P M FitzGerald1, J Jankovic, A K Percy.   

Abstract

Rett syndrome, a progressive neurodegenerative disorder described only in female subjects, is manifested by a wide spectrum of behavioral and motor abnormalities. We studied 32 patients with this disorder, ages 30 months to 28 years old, and characterized their extrapyramidal disturbance. The most common motor abnormalities were stereotyped movements and gait disturbance, seen in all patients. Bruxism, oculogyric crises, parkinsonism, and dystonia were also common, but myoclonus and choreoathetosis were seen only infrequently. The hyperkinetic movement disorders tended to dominate in younger patients, while bradykinetic disorders were more evident in the older patients. This study provides evidence that movement disorders seen in Rett syndrome reflect age-related neurodegenerative changes in the basal ganglia.

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Year:  1990        PMID: 2388636     DOI: 10.1002/mds.870050303

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


  31 in total

1.  The course of awake breathing disturbances across the lifespan in Rett syndrome.

Authors:  Daniel C Tarquinio; Wei Hou; Jeffrey L Neul; Gamze Kilic Berkmen; Jana Drummond; Elizabeth Aronoff; Jennifer Harris; Jane B Lane; Walter E Kaufmann; Kathleen J Motil; Daniel G Glaze; Steven A Skinner; Alan K Percy
Journal:  Brain Dev       Date:  2018-04-12       Impact factor: 1.961

2.  Clinical severity and quality of life in children and adolescents with Rett syndrome.

Authors:  J B Lane; H-S Lee; L W Smith; P Cheng; A K Percy; D G Glaze; J L Neul; K J Motil; J O Barrish; S A Skinner; F Annese; L McNair; J Graham; O Khwaja; K Barnes; J P Krischer
Journal:  Neurology       Date:  2011-10-19       Impact factor: 9.910

3.  Loss of Mecp2 in substantia nigra dopamine neurons compromises the nigrostriatal pathway.

Authors:  Stephanie C Gantz; Christopher P Ford; Kim A Neve; John T Williams
Journal:  J Neurosci       Date:  2011-08-31       Impact factor: 6.167

4.  Level of purposeful hand function as a marker of clinical severity in Rett syndrome.

Authors:  Jenny Downs; Ami Bebbington; Peter Jacoby; Anne-Marie Williams; Soumya Ghosh; Walter E Kaufmann; Helen Leonard
Journal:  Dev Med Child Neurol       Date:  2010-03-19       Impact factor: 5.449

Review 5.  Mouse models of neurodevelopmental disease of the basal ganglia and associated circuits.

Authors:  Samuel S Pappas; Daniel K Leventhal; Roger L Albin; William T Dauer
Journal:  Curr Top Dev Biol       Date:  2014       Impact factor: 4.897

6.  A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical Trials.

Authors:  Melissa Raspa; Carla M Bann; Angela Gwaltney; Timothy A Benke; Cary Fu; Daniel G Glaze; Richard Haas; Peter Heydemann; Mary Jones; Walter E Kaufmann; David Lieberman; Eric Marsh; Sarika Peters; Robin Ryther; Shannon Standridge; Steven A Skinner; Alan K Percy; Jeffrey L Neul
Journal:  Am J Intellect Dev Disabil       Date:  2020-11-01

7.  Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective.

Authors:  Marisela E Dy; Jeff L Waugh; Nutan Sharma; Heather O'Leary; Kush Kapur; Alissa M D'Gama; Mustafa Sahin; David K Urion; Walter E Kaufmann
Journal:  Pediatr Neurol       Date:  2017-06-02       Impact factor: 3.372

Review 8.  Phelan-McDermid Syndrome and SHANK3: Implications for Treatment.

Authors:  Jesse L Costales; Alexander Kolevzon
Journal:  Neurotherapeutics       Date:  2015-07       Impact factor: 7.620

9.  Inflammatory protein response in CDKL5-Rett syndrome: evidence of a subclinical smouldering inflammation.

Authors:  Alessio Cortelazzo; Claudio de Felice; Silvia Leoncini; Cinzia Signorini; Roberto Guerranti; Roberto Leoncini; Alessandro Armini; Luca Bini; Lucia Ciccoli; Joussef Hayek
Journal:  Inflamm Res       Date:  2016-11-29       Impact factor: 4.575

10.  Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndrome.

Authors:  Jonathan K Merritt; Bridget E Collins; Kirsty R Erickson; Hongwei Dong; Jeffrey L Neul
Journal:  Hum Mol Genet       Date:  2020-08-29       Impact factor: 6.150

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