Though Rett syndrome is genetic, it isn't inherited from either parent. Instead, it's caused by a gene mutation. Children ...

Rett syndrome is caused by mutations of the MECP2 gene located on the X chromosome. Children with Rett initially show typical ...

I’m thrilled to join the Board of Trustees and get even closer to the Reverse Rett mission,” says Amy Gilliland. “As a parent of a child living with Rett syndrome—like so many others leading and ...

The medical aspects of Rett syndrome (RS) require careful attention, particularly, nutrition, gastrointestinal function, epilepsy and scoliosis. Longevity is better understood, with survival ...

In the literature, the reported detection rate for MECP2 mutations in patients with clinically defined Rett syndrome is between 60% and 80%. It is obvious that these rates are influenced by the ...

An experimental cancer drug could make thinking easier for individuals with Rett syndrome, a rare disorder linked to autism, according to new research from the University of California San Diego ...

Rett syndrome is a rare genetic disease affecting 1 in 10,000 newborn girls, characterised by sudden regression around 1 year of age, with loss of acquired language and motor skills and leading to ...

Rett syndrome is a rare genetic disease affecting ... and leading to profound cognitive impairment. Its main cause is mutations of the gene MeCP2, an important controller of neuronal development ...

Phase 2a TREE study assesses safety and efficacy of leriglitazone Minoryx Therapeutics has dosed the first patient in its phase 2a TREE study, which evaluates the safety and efficacy of leriglitazone ...

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 ...