Horus’ VECTrans® platform to deliver Servier’s oligonucleotides to the brain for the treatment of rare neurological and ...

For years, it has been known that mutations in both copies of the HERC2 gene are associated with a neurodevelopmental disorder characterized by global developmental delay, intellectual disability, ...

Different neuropsychiatric and neurodevelopmental conditions, such as schizophrenia, bipolar disorder, ...

Differences in brain connectivity are linked to several neurodevelopmental disorders, yet scientists still struggle to determine what changes are shared or unique to each condition. A new study ...

At Children's Hospital Colorado, Aurora, Colorado, pediatricians will soon have a new ally in diagnosing and identifying complex neurodevelopmental conditions like ...

The Manton Center works with over 3,500 patients globally who are affected by rare diseases. Brownstein, one of the study's ...

Adding genetic testing to the evaluation of pediatric patients with neurodevelopmental disorders (NDD) resulted in more individualized care. Adding genetic testing to the evaluation of pediatric ...

A research team from National Taiwan University and the University of Oslo analyzed data on more than 1.3 million children across two countries, finding that an earlier European safety warning for ...

Researchers have found that motor delay and low muscle tone were common signs of an underlying genetic diagnosis in children with neurodevelopment disorders. In a new study, UCLA Health researchers ...

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 ...