Aim: To identify the clinical features correlating with the presence and severity of scoliosis in girls with Rett syndrome (RTT). Method: Seventy-five girls with a clinical and genetically determined diagnosis of RTT participated in this cross-sectional study. Clinical scales administered included the Rett assessment rating scale, the modified Ashworth scale, the Rett syndrome motor evaluation scale, the PainAD, and the scale of evaluation of purposeful hand function. Multivariable analyses, such as ordinal logistic regression and ANCOVA, were used to assess the correlation between these scales and a clinical score of scoliosis. Results: About 60% of patients had scoliosis, in general mild or moderate. The severity of scoliosis correlated w...
Rett syndrome (RTT) is a neurodevelopmental disorder impacting 1 in 10,000 females worldwide, making...
© 2016 Downs et al. Rett syndrome is a pervasive neurodevelopmental disorder associated with a path...
Objective: Rett syndrome is a rare neurodevelopmental disorder that is usually associated with a mut...
Population-based longitudinal observational study.To describe the prevalence of scoliosis in Rett sy...
STUDY DESIGN.: Population-based longitudinal observational study. OBJECTIVES.: To describe the preva...
Study Design. Population-based longitudinal observational study. Objective. To describe the prevalen...
Aim To describe a new clinical tool, the Rett Syndrome Motor Evaluation Scale (RESMES) and to assess...
Rett syndrome is a genetic disorder primarily affecting females. One of its most disabling features ...
Objective. To develop guidelines for the clinical man-agement of scoliosis in Rett syndrome through ...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
Study Design.: Modified Delphi technique. Objective.: To develop guidelines for the clinical managem...
This study aimed to determine whether there is a relationship between abnormal foot position and sta...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
Aim - We investigated relationships between hand function and genotype and aspects of phenotype in R...
Rett syndrome (RTT) is a neurodevelopmental disorder impacting 1 in 10,000 females worldwide, making...
© 2016 Downs et al. Rett syndrome is a pervasive neurodevelopmental disorder associated with a path...
Objective: Rett syndrome is a rare neurodevelopmental disorder that is usually associated with a mut...
Population-based longitudinal observational study.To describe the prevalence of scoliosis in Rett sy...
STUDY DESIGN.: Population-based longitudinal observational study. OBJECTIVES.: To describe the preva...
Study Design. Population-based longitudinal observational study. Objective. To describe the prevalen...
Aim To describe a new clinical tool, the Rett Syndrome Motor Evaluation Scale (RESMES) and to assess...
Rett syndrome is a genetic disorder primarily affecting females. One of its most disabling features ...
Objective. To develop guidelines for the clinical man-agement of scoliosis in Rett syndrome through ...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
Study Design.: Modified Delphi technique. Objective.: To develop guidelines for the clinical managem...
This study aimed to determine whether there is a relationship between abnormal foot position and sta...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
Aim - We investigated relationships between hand function and genotype and aspects of phenotype in R...
Rett syndrome (RTT) is a neurodevelopmental disorder impacting 1 in 10,000 females worldwide, making...
© 2016 Downs et al. Rett syndrome is a pervasive neurodevelopmental disorder associated with a path...
Objective: Rett syndrome is a rare neurodevelopmental disorder that is usually associated with a mut...