Latest disorder Stories
An estimated 2.2 million people in the United States live with epilepsy, a complex brain disorder characterized by sudden and often unpredictable seizures.
Autism is a highly heritable neurodevelopmental disorder, yet the genetic underpinnings in the brain at young ages have remained largely unknown.
A select number of patients who suffer from neurally mediated synope (NMS) – a disorder in which the brain fails to regulate heart rate and blood pressure – may be good candidates to receive a dual-chamber pacemaker to prevent common NMS-related fainting spells.
A study led by Eric Courchesne, PhD, director of the Autism Center of Excellence at the University of California, San Diego School of Medicine has, for the first time, identified in young autism patients genetic mechanisms involved in abnormal early brain development and overgrowth that occurs in the disorder.
The youngest children in the classroom are significantly more likely to be diagnosed with attention-deficit/hyperactivity disorder (ADHD) — and prescribed medication — than their peers in the same grade.
Researchers have identified a gene that causes adult-onset primary cervical dystonia, an often-painful condition in which patients' necks twist involuntarily.
Millions of people suffer from Parkinson's disease, a disorder of the nervous system that affects movement and worsens over time.
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