Rett syndrome is a rare neurological and developmental disorder that leads to a gradual decline in motor skills and language.

A new UC Davis MIND Institute study offers critical insights into Rett syndrome, a rare genetic condition that ... and during ...

over placebo in children with Rett syndrome – a devastating neurological disorder caused by mutations in the MECP2 gene found on the X chromosome. The disease causes deficits in brain function ...

Rett syndrome is a devastating neurological disorder caused mainly by mutations in the MECP2 gene found on the X chromosome. The disease causes deficits in brain function that lead to behavioural ...

Indeed, REL-1017 also has significant potential in multiple additional central nervous system conditions, including movement disorders and Rett syndrome, a rare neurological disorder affecting ...

A new mega-database of half a million mutations may flag new ways of treating genetic disease, scientists say.

Taysha Gene Therapies' TSHA-102 tackles Rett syndrome’s root cause with its ... You see, Rett is an extremely rare disorder that’s also prevalent in women due to MECP2 gene mutations.

These initiatives represent a way to accelerate access to treatments that have historically faced longer regulatory pathways.

and rare diseases, including Rett syndrome, and other central nervous system (CNS) disorders, today announced that The Journal of Prevention of Alzheimer’s Disease (JPAD) has published peer ...