Background: The clinical characteristics of children diagnosed with Rett syndrome are well described. Survival and how these characteristics persist or change in adulthood are less well documented. This study aimed to describe overall survival and adult health in those with Rett syndrome.Methods: Using the Kaplan-Meier method, we estimated survival of individuals registered with the Australian Rett syndrome Database (ARSD) who had been followed for up to 20 years (n = 396). We then conducted logistic and linear regression analyses investigating epilepsy, musculoskeletal, gastrointestinal, autonomic dysfunction and behaviour of individuals aged 18 years and over using cross sectional cohorts from the ARSD (n = 150) and the international data...
Modifications to diagnostic criteria and introduction of genetic testing have likely affected the pa...
ObjectiveRett syndrome is a severe neurodevelopmental disorder affecting approximately one in 10,000...
Background: Rett Syndrome (RTT) is a rare, neurodevelopmental disorder characterised by a range of p...
Background: The clinical characteristics of children diagnosed with Rett syndrome are well described...
BACKGROUND: Little is known about the aging process of people with specific syndromes, like Rett syn...
Survival in Rett syndrome remains unclear. Although early estimates were grim, more recent data sugg...
Purpose Survival in Rett syndrome remains unclear. Although early estimates were grim, more recent d...
Background: The aim was to gain a UK national sample of people with Rett syndrome across the age ran...
Purpose: Rett syndrome (RTT) is a neurodevelopmental disorder that almost exclusively affects female...
Rett syndrome (RTT) is a rare neurodevelopmental disorder, linked to MECP2 gene mutations in the maj...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
Background Rett syndrome is a complex genetic disorder with age-specific manifestations and over hal...
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...
Rett syndrome (RTT) is a neurodevelopmental disorder which is characterized by an apparently normal ...
Modifications to diagnostic criteria and introduction of genetic testing have likely affected the pa...
ObjectiveRett syndrome is a severe neurodevelopmental disorder affecting approximately one in 10,000...
Background: Rett Syndrome (RTT) is a rare, neurodevelopmental disorder characterised by a range of p...
Background: The clinical characteristics of children diagnosed with Rett syndrome are well described...
BACKGROUND: Little is known about the aging process of people with specific syndromes, like Rett syn...
Survival in Rett syndrome remains unclear. Although early estimates were grim, more recent data sugg...
Purpose Survival in Rett syndrome remains unclear. Although early estimates were grim, more recent d...
Background: The aim was to gain a UK national sample of people with Rett syndrome across the age ran...
Purpose: Rett syndrome (RTT) is a neurodevelopmental disorder that almost exclusively affects female...
Rett syndrome (RTT) is a rare neurodevelopmental disorder, linked to MECP2 gene mutations in the maj...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
Background Rett syndrome is a complex genetic disorder with age-specific manifestations and over hal...
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...
Rett syndrome (RTT) is a neurodevelopmental disorder which is characterized by an apparently normal ...
Modifications to diagnostic criteria and introduction of genetic testing have likely affected the pa...
ObjectiveRett syndrome is a severe neurodevelopmental disorder affecting approximately one in 10,000...
Background: Rett Syndrome (RTT) is a rare, neurodevelopmental disorder characterised by a range of p...