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This study investigated the nature and prevalence of atypical pain responses in Rett syndrome and their relationships with specific MECP2 mutations.
Physical and mental health in mothers of children with Down syndrome.
Rett syndrome (RTT) is an X-linked dominant neurodevelopmental disorder that is usually associated with mutations in the MECP2 gene.
Feeding difficulties in Rett syndrome are complex and multifactorial. In this study, we describe the feeding experiences in Rett syndrome and examine the...
To examine the prevalence, cumulative incidence, and survival in an Australian cohort with Rett syndrome (RTT).
To investigate specific child and parental factors associated with increased vulnerability to substantiated child maltreatment.
Stereotypic hand movements are a feature of Rett Syndrome but few studies have observed their nature systematically.
Annual economic cost of Duchenne Muscular Dystrophy was found to be high, reflecting a significant socioeconomic burden, especially in boys who reach adulthood
Perspectives of parents are integral to the assessment of communication abilities and inform communication interventions for girls and women with Rett Syndrome
Scoliosis is a common clinical manifestation of Rett syndrome, a neurodevelopmental disorder that almost exclusively affects girls.