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Showing results for "preterm birth lungs"
Fourteen of 74 Chinese families known to the International Rett Syndrome Phenotype Database participated in this qualitative study.
The diagnosis of a rare disorder is dependent on the clinician's particular knowledge and experience, and can be challenging when the presentation is variable.
This study describes the attainment of gross developmental milestones and regression, and assesses the relationships between genotype and age at diagnosis.
There is often delay between onset of Rett syndrome symptoms and its diagnosis, possibly related to symptom presentation or socio-demographic factors.
To develop guidelines for the clinical management of scoliosis in Rett syndrome through evidence review and consensus expert panel opinion.
Scoliosis is the most common orthopaedic complication of Rett syndrome. Parents of affected individuals are vital partners in the clinical management...
This paper describes the development of a video-based evaluation tool for use in Rett syndrome (RTT).
To investigate how well intellectual disability (ID) can be ascertained using hospital morbidity data compared with a population-based data source.
This cross-sectional study examined parental well-being in caregivers of children with one of three genetic disorders associated with intellectual disability.
We aimed to: (1) describe the patterns of sedentary time and daily steps and (2) identify the association of individual and environmental characteristitics.