Literature DB >> 2344020

Characteristics of motor disturbances of the Rett syndrome.

Y Nomura1, M Segawa.   

Abstract

The stereotyped movement of hands, one of the core symptoms of the Rett syndrome (RS), was analyzed to study the pathophysiology. The development of hand function was delayed after mid-infancy and handedness was undetermined in most cases. Before the onset of the pathognomonic stereotypy, patients showed excessive or abnormal behaviors of hands and mouth, such as patting or licking hands, etc. The useful hand function was lost just before or after the onset of stereotypy. The characteristic "hand wringing" movement at midline became apparent from 8 months to 3 years of age. The synchronous hand movement without reaching the midline and leg movement at midline were also seen in some patients. Based on the analysis of these symptoms, it is suggested that the stereotyped movements of RS are manifestation of fragments of normal motor behaviors at immature levels appearing excessively and repetitively with the abnormal basic posture. The pathophysiological mechanism of these characteristics is thought to be due to the hypofunctional state of the monoaminergic system from early ontogeny, which is in accordance with our previous hypothesis that RS is a developmental disorder of the monoaminergic system. The roles of the cortical involvement and sensory system are also discussed.

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Mesh:

Year:  1990        PMID: 2344020     DOI: 10.1016/s0387-7604(12)80170-7

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  5 in total

1.  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

2.  Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis.

Authors:  Daniel C Tarquinio; Wei Hou; Jeffrey L Neul; Jane B Lane; Katherine V Barnes; Heather M O'Leary; Natalie M Bruck; Walter E Kaufmann; Kathleen J Motil; Daniel G Glaze; Steven A Skinner; Fran Annese; Lauren Baggett; Judy O Barrish; Suzanne P Geerts; Alan K Percy
Journal:  Pediatr Neurol       Date:  2015-02-16       Impact factor: 3.372

3.  MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats.

Authors:  Kelsey C Patterson; Virginia E Hawkins; Kara M Arps; Daniel K Mulkey; Michelle L Olsen
Journal:  Hum Mol Genet       Date:  2016-06-21       Impact factor: 6.150

4.  Oral health experiences of individuals with Rett syndrome: a retrospective study.

Authors:  Y Y L Lai; K Wong; N M King; J Downs; H Leonard
Journal:  BMC Oral Health       Date:  2018-11-29       Impact factor: 2.757

5.  Gait analysis in a Mecp2 knockout mouse model of Rett syndrome reveals early-onset and progressive motor deficits.

Authors:  Kamal K E Gadalla; Paul D Ross; John S Riddell; Mark E S Bailey; Stuart R Cobb
Journal:  PLoS One       Date:  2014-11-13       Impact factor: 3.240

  5 in total

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