Aim - We investigated relationships between hand function and genotype and aspects of phenotype in Rett syndrome. Method - Video assessment in naturalistic settings was supplemented by parent-reported data in a cross-sectional study of 144 females with a mean age of 14 years 10 months (SD 7y 10mo; range 2y–31y 10mo), 110 of whom had a mutation of the methyl CpG binding protein 2 (MECP2) gene. Ordinal logistic regression was used to assess relationships between hand function and MECP2 mutation, age, a modified Kerr score, Functional Independence Measure for Children (WeeFIM), ambulation level, and frequency of hand stereotypies. Results - Approximately two-thirds of participants demonstrated purposeful hand function, ranging from simple gras...
Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the...
Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the...
Background: The diagnosis of Rett syndrome (RTT) is based on a set of clinical criteria, irrespectiv...
Abstract: Objective: We aimed to determine the longitudinal distribution of hand function skills i...
Objective: Rett syndrome is a rare neurodevelopmental disorder that is usually associated with a mut...
Loss of hand function is a core feature of Rett syndrome. This article describes longitudinal hand f...
Loss of hand function is a core feature of Rett syndrome. This article describes longitudinal hand f...
BackgroundRett syndrome (RTT), a neurodevelopmental disorder that primarily affects girls, is charac...
Hand stereotypies are considered a hallmark of Rett syndrome (RTT) and are usually described as symm...
Aim To describe a new clinical tool, the Rett Syndrome Motor Evaluation Scale (RESMES) and to assess...
© 2016 Downs et al. Rett syndrome is a pervasive neurodevelopmental disorder associated with a path...
Aim: To identify the clinical features correlating with the presence and severity of scoliosis in gi...
Background: Rett syndrome is a progressive neurodevelopment disorder which mainly affects females an...
Although physical features, including loss of hand skills, deceleration of head growth, spasticity a...
We aimed to improve the understanding of genotype-phenotype correlations in Rett syndrome (RS) by ad...
Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the...
Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the...
Background: The diagnosis of Rett syndrome (RTT) is based on a set of clinical criteria, irrespectiv...
Abstract: Objective: We aimed to determine the longitudinal distribution of hand function skills i...
Objective: Rett syndrome is a rare neurodevelopmental disorder that is usually associated with a mut...
Loss of hand function is a core feature of Rett syndrome. This article describes longitudinal hand f...
Loss of hand function is a core feature of Rett syndrome. This article describes longitudinal hand f...
BackgroundRett syndrome (RTT), a neurodevelopmental disorder that primarily affects girls, is charac...
Hand stereotypies are considered a hallmark of Rett syndrome (RTT) and are usually described as symm...
Aim To describe a new clinical tool, the Rett Syndrome Motor Evaluation Scale (RESMES) and to assess...
© 2016 Downs et al. Rett syndrome is a pervasive neurodevelopmental disorder associated with a path...
Aim: To identify the clinical features correlating with the presence and severity of scoliosis in gi...
Background: Rett syndrome is a progressive neurodevelopment disorder which mainly affects females an...
Although physical features, including loss of hand skills, deceleration of head growth, spasticity a...
We aimed to improve the understanding of genotype-phenotype correlations in Rett syndrome (RS) by ad...
Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the...
Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the...
Background: The diagnosis of Rett syndrome (RTT) is based on a set of clinical criteria, irrespectiv...