Rett syndrome (RTT) is a genetic disorder that typically becomes apparent after 6–18 months of age and almost exclusively in females. Symptoms include...

She is known for establishing the UK's Rett Clinic for children with the neurodevelopmental disorder Rett syndrome, developing palliative care for children...

Currently there is no cure for Rett syndrome. Treatment is directed towards improving function and addressing symptoms throughout life. A multi-disciplinary...

genetic defect of the transcriptional regulator MECP2 is responsible for Rett syndrome. A MECP2 deficiency has been associated to catecholaminergic dysfunctions...

spectrum disorder, childhood disintegrative disorder, Rett syndrome, Landau-Kleffner syndrome, and neuro-degenerative diseases. The loss of motor, language...

palsy Rett syndrome Mowat–Wilson syndrome Adenylosuccinate lyase deficiency Pitt–Hopkins syndrome Phelan–McDermid syndrome Prader–Willi syndrome There...

responsible for a number of devastating neurological disorders, such as Rett syndrome and spinocerebellar ataxia type 1. Zoghbi's discoveries have provided...

X inactivation. MECP2 gene mutations are the cause of most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most...

potentially be separate events, or both be caused by an unknown source. Rett syndrome is a genetic disorder caused by a mutation of the MECP2 gene on the...

syndrome can be marked by intellectual disabilities as well as problems with socializing. It is part of the clinical spectrum of Rett-like syndromes....