Researchers have developed an artificial intelligence (AI) approach that accelerates the identification of genes that contribute to neurodevelopmental conditions such as autism spectrum disorder, ...

Schinzel–Giedion syndrome (SGS), caused by missense variants in the degron region, leading to toxic gain-of-function. SETBP1 haploinsufficiency, typically caused by truncating mutations or deletions.

For babies born with alternative hemiplegia of childhood (AHC), an extremely rare and severe neurodevelopmental disorder, there may be no obvious symptoms for several months. Then the attacks begin: ...

Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, affecting 12%–13% of adolescents in the United States, according to some studies. The pattern of inattention, ...

Jane, Julie, and Jemma are 6-year-old classmates. The three girls show several similarities in behaviour and cognition. All three struggle with starting new tasks, task-switching, sustaining attention ...

Pathologic changes of the X-chromosome gene for dystrophin give rise to Duchenne muscular dystrophy (DMD), and dystrophin -- which minimizes muscle fiber loss due to sarcolemma contraction damage when ...

Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, affecting 12%–13% of adolescents in the United States, according to some studies.

Harvard Medical School and Massachusetts General Hospital researchers found a correlation between Covid-19 infection contracted during pregnancy and risk of neurodevelopmental disorders in offspring ...

In line with the vision of Sustainable Development Goal 3 that promotes mental health and well-being for individuals of all ages, the Department of Clinical Psychology at Srinivas University, under ...