Add to ORKGRett syndrome is a rare genetic neurodevelopmental disorder. Cross sectional and longitudinal densitometry assessment in Rett syndrome found decreased bone density with age but muscle mass and mensus afforded some protection. Consensus-based clinical management guidelines provided recommendations for clinical assessment and pharmacological and non-pharmacological interventions. These data have the potential to reduce the frequency of fractures in Rett syndrome and stimulate further research that aims to ameliorate the impacts of poor bone health
Rett syndrome, an X-linked neurodevelopmental disorder primarily affecting girls, is frequently char...
Rett syndrome is a common X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene...
Rett syndrome is a severe neurodevelopmental disorder affecting girls, caused by mutations in the ME...
Objectives We developed clinical guidelines for the management of bone health in Rett syndrome throu...
ObjectivesWe developed clinical guidelines for the management of bone health in Rett syndrome throug...
Bone mass and density are low in females with Rett syndrome. This study used Dual energy x-ray absor...
Osteoporosis is the reduction of calcium density in bones, usually evident in postmenopausal females...
Objectives - We developed clinical guidelines for the management of bone health in Rett syndrome thr...
Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-li...
Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-li...
The aim of the present study was to characterize biomarkers of bone turnover and their relation with...
Background: Low bone mass is a frequent and early complication of girls with Rett syndrome. As a con...
This study evaluated bone status and bone turnover in 82 females (ages 2-21 years) with the Rett Syn...
Background: More than 95% of individuals with RTT have mutations in methyl-CpG-binding protein 2 (ME...
Rett syndrome, an X-linked neurodevelopmental disorder primarily affecting girls, is frequently char...
Rett syndrome is a common X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene...
Rett syndrome is a severe neurodevelopmental disorder affecting girls, caused by mutations in the ME...
Objectives We developed clinical guidelines for the management of bone health in Rett syndrome throu...
ObjectivesWe developed clinical guidelines for the management of bone health in Rett syndrome throug...
Bone mass and density are low in females with Rett syndrome. This study used Dual energy x-ray absor...
Osteoporosis is the reduction of calcium density in bones, usually evident in postmenopausal females...
Objectives - We developed clinical guidelines for the management of bone health in Rett syndrome thr...
Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-li...
Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-li...
The aim of the present study was to characterize biomarkers of bone turnover and their relation with...
Background: Low bone mass is a frequent and early complication of girls with Rett syndrome. As a con...
This study evaluated bone status and bone turnover in 82 females (ages 2-21 years) with the Rett Syn...
Background: More than 95% of individuals with RTT have mutations in methyl-CpG-binding protein 2 (ME...
Rett syndrome, an X-linked neurodevelopmental disorder primarily affecting girls, is frequently char...
Rett syndrome is a common X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene...
Rett syndrome is a severe neurodevelopmental disorder affecting girls, caused by mutations in the ME...