Gross Motor Profile in Rett Syndrome as Determined by Video Analysis

被引:52
作者
Downs, J. A. [1 ]
Bebbington, A. [1 ]
Jacoby, P. [1 ]
Msall, M. E. [2 ,3 ,4 ]
McIlroy, O. [1 ]
Fyfe, S. [5 ]
Bahi-Buisson, N. [6 ]
Kaufmann, W. E. [7 ,8 ]
Leonard, H. [1 ]
机构
[1] Univ Western Australia, Ctr Child Hlth Res, Telethon Inst Child Hlth Res, Perth, WA 6872, Australia
[2] Univ Chicago, Comer Childrens Hosp, Kennedy Ctr Intellectual & Dev Disabil, Inst Mol Pediat Sci, Chicago, IL USA
[3] Univ Chicago, LaRabida Childrens Hosp, Kennedy Ctr Intellectual & Dev Disabil, Inst Mol Pediat Sci, Chicago, IL USA
[4] Univ Chicago, Sect Dev & Behav Pediat, Chicago, IL USA
[5] Curtin Univ Technol, Sch Publ Hlth, Perth, WA, Australia
[6] Univ Paris 05, INSERM, U663, Necker Enfants Malad Hosp Paris, F-75270 Paris 06, France
[7] Kennedy Krieger Inst, Ctr Genet Disorders Cognit & Behav, Baltimore, MD USA
[8] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
基金
澳大利亚国家健康与医学研究理事会;
关键词
Rett syndrome; gross motor function; mobility; movement disorder; MECP2; mutation; phenotype;
D O I
10.1055/s-0028-1104575
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Movement impairment is a fundamental but variable component of the Rett syndrome phenotype. This study used video supplemented by parent report data to describe the gross motor profile in females with Rett syndrome (n = 99) and to investigate the impact of age, genotype, scoliosis and hand stereotypies. Factor analysis enabled the calculation of general and complex gross motor skills scores. Most subjects were able to sit, slightly less than half were able to walk and a minority were able to transfer without assistance. General gross motor skills declined with age and were poorer in those who had surgically treated scoliosis but not conservatively managed scoliosis. Complex gross motor skills did not decline with age and were better in those without scoliosis. Those with a p.R133C, p.R294X, or a p.R255X mutation appear to have better motor skills overall than those with a p.R270X or large deletion mutation. Motor scores were not related to the frequency of hand stereotypies. This information is useful for the clinician and family when planning Support strategies and interventions.
引用
收藏
页码:205 / 210
页数:6
相关论文
共 32 条
[1]   Predictors of scoliosis in Rett syndrome [J].
Ager, Sarah ;
Fyfe, Susan ;
Christodoulou, John ;
Jacoby, Peter ;
Schmitt, Lincoln ;
Leonard, Helen .
JOURNAL OF CHILD NEUROLOGY, 2006, 21 (09) :809-813
[2]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[3]   Speech and motor disturbances in Rett syndrome [J].
Bashina V.M. ;
Simashkova N.V. ;
Grachev V.V. ;
Gorbachevskaya N.L. .
Neuroscience and Behavioral Physiology, 2002, 32 (4) :323-327
[4]   Investigating genotype-phenotype relationships in Rett syndrome using an international data set [J].
Bebbington, A. ;
Anderson, A. ;
Ravine, D. ;
Fyfe, S. ;
Pineda, M. ;
de Klerk, N. ;
Ben-Zeev, B. ;
Yatawara, N. ;
Percy, A. ;
Kaufmann, W. E. ;
Leonard, H. .
NEUROLOGY, 2008, 70 (11) :868-875
[5]   Findings from a multidisciplinary clinical case series of females with Rett syndrome [J].
Cass, H ;
Reilly, S ;
Owen, L ;
Wisbeach, A ;
Weekes, L ;
Slonims, V ;
Wigram, T ;
Charman, T .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2003, 45 (05) :325-337
[6]   Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndrome [J].
Charman, T ;
Neilson, TC ;
Mash, V ;
Archer, H ;
Gardiner, MT ;
Knudsen, GPS ;
McDonnell, A ;
Perry, J ;
Whatley, SD ;
Bunyan, DJ ;
Ravn, K ;
Mount, RH ;
Hastings, RP ;
Hulten, M ;
Orstavik, KH ;
Reilly, S ;
Cass, H ;
Clarke, A ;
Kerr, AM ;
Bailey, MES .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (10) :1121-1130
[7]   Refining the phenotype of common mutations in Rett syndrome [J].
Colvin, L ;
Leonard, H ;
de Klerk, N ;
Davis, M ;
Weaving, L ;
Williamson, S ;
Christodoulou, J .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (01) :25-30
[8]   Describing the phenotype in Rett syndrome using a population database [J].
Colvin, L ;
Fyfe, S ;
Leonard, S ;
Schiavello, T ;
Ellaway, C ;
de Klerk, N ;
Christodoulou, J ;
Msall, M ;
Leonard, H .
ARCHIVES OF DISEASE IN CHILDHOOD, 2003, 88 (01) :38-43
[9]   RETT SYNDROME AND ASSOCIATED MOVEMENT-DISORDERS [J].
FITZGERALD, PM ;
JANKOVIC, J ;
PERCY, AK .
MOVEMENT DISORDERS, 1990, 5 (03) :195-202
[10]   Development of a video-based evaluation tool in rett syndrome [J].
Fyfe, S. ;
Downs, J. ;
McIlroy, O. ;
Burford, B. ;
Lister, J. ;
Reilly, S. ;
Laurvick, C. L. ;
Philippe, C. ;
Msall, M. ;
Kaufmann, W. E. ;
Ellaway, C. ;
Leonard, H. .
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 2007, 37 (09) :1636-1646