UCLA Health researchers say study findings uncover Huntington's disease mechanisms and pave new ways to develop treatments.

Huntington's disease is a rare genetic, autosomal dominant, neurodegenerative disease, caused by CAG repeat expansions in the HTT gene, that is polymorphic on the healthy allele and contains more than ...

What initially seems like purely psychological trouble may indeed have roots in physical conditions that, once identified, ...

Federally funded research at Johns Hopkins offers new avenues for detecting brain disease long before it strikes ...

Biosciences presented data from the KINECT-HD study showcasing significant improvements in chorea across body regions with ...

Medically reviewed by Smita Patel, DO Bradykinesia is a progressive movement symptom commonly found in people with ...

The late Maggie Fee was remembered with a cheque presentation for £250 raised in her name that was made to a representative of ...

Despite its increasing prevalence, a painful condition called bladder pain syndrome, or interstitial cystitis, remains ...

According to the University of California San Francisco, Huntington’s disease affects one in every 10,000 to 20,000 people in ...

Neurological motor disorders (NMDs) such as Parkinson's disease and Huntington's disease are characterized by the accumulation and aggregation of misfolded proteins that trigger cell death of specific ...