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If you haven't heard of Rett syndrome, it's probably because it's very rare. Affecting an estimated one in 12,000 baby girls ...
1 Program in Developmental Biology, the Hospital for Sick Children, Toronto, Canada 2 Western Sydney Genetics Program, the Royal Alexandra Hospital for Children, Sydney, and Discipline of Paediatrics ...
Rett syndrome is a neurodevelopmental disorder that primarily affects girls, most of whom have mutations in the transcription regulatory gene MECP2. However, mutations in MECP2 also have been ...
Rett syndrome (RS) is an incurable neurological disorder that occurs in females. Although the biological basis is unknown, there is substantial evidence suggesting a genetic basis. RS is ...
Rett syndrome is a unique and severe postnatal neurological disorder which mainly affects mostly girls. However, it may rarely affect boys. This condition is generally discovered during the first two ...
A recent collaborative study has discovered rare variants in the YKT6 gene as the cause of a new neurological disorder characterized by developmental delays along with severe progressive liver ...
1 Centre for Child Health Research, The University of Western Australia, Telethon Institute for Child Health Research, Perth, Western Australia 2 Curtin University of Technology, Perth, Western ...
With the FDA’s first approval for a treatment for Rett syndrome now under its belt, Daybue maker Acadia Pharmaceuticals has debuted its latest effort to raise awareness around the rare disease.
THE final annual 127-mile walk to help people with a rare neurological disorder has raised more than £3,500. The arduous Walk for Estelle along the full length of the Leeds and Liverpool Canal was ...