Document Detail


Longitudinal hand function in rett syndrome.
MedLine Citation:
PMID:  20921565     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Loss of hand function is a core feature of Rett syndrome. This article describes longitudinal hand function at 3 time points for 72 subjects participating in the Australian Rett Syndrome Database. Approximately 40% of subjects with some grasping abilities lost skill over the 3- to 4-year period between video assessments. In these subjects, a decrease in hand function was seen less frequently in girls 13 to 19 years old than in those younger than 8 years, in subjects with some mobility compared with those who were wheelchair bound, and in those who had previously been able to finger feed. Relationships with the magnitude of change reflected these findings. Change in hand function did not vary with clinical severity. The results for all subjects were similar to results obtained when analysis was restricted to those with a pathogenic mutation. Variability in the longitudinal course of hand function in Rett syndrome was observed.
Authors:
Jennepher Downs; Ami Bebbington; Walter E Kaufmann; Helen Leonard
Related Documents :
2531225 - Pituitary function studies in a case of mild hunter's syndrome (mps iib).
21056055 - Motor problems in prader-willi syndrome: a systematic review on body composition and ne...
8156125 - Esophagectomy without thoracotomy with vagal preservation.
11509785 - Laparoscopic creation of a neovagina in mayer-rokitansky-kuster-hauser syndrome by modi...
20430655 - A patient with digeorge syndrome with spina bifida and sacral myelomeningocele, who dev...
17311705 - A case of oxaliplatin-related posterior reversible encephalopathy syndrome.
Publication Detail:
Type:  Journal Article     Date:  2010-10-04
Journal Detail:
Title:  Journal of child neurology     Volume:  26     ISSN:  1708-8283     ISO Abbreviation:  J. Child Neurol.     Publication Date:  2011 Mar 
Date Detail:
Created Date:  2011-03-08     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8606714     Medline TA:  J Child Neurol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  334-40     Citation Subset:  IM    
Affiliation:
Telethon Institute for Child Health Research, Centre for Child Health Research, The University of Western Australia, Perth, Western Australia, School of Physiotherapy and Curtin Health Innovation Research Institute, Curtin University of Technology, Perth, Western Australia.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Slow wave activity during sleep: functional and therapeutic implications.
Next Document:  Congenital hypotonia in a child with a de novo 22q13 monosomy and 2pter duplication: a clinical and ...