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Huntington's Disease: Hope Through Research

Introduction
What Causes Huntington’s Disease?
How is HD Inherited?
What are the Major Effects of the Disease?
At What Age Does HD Appear?
How is HD Diagnosed?
What is Presymptomatic Testing?
How is the Presymptomatic Test Conducted?
How Does a Person Decide Whether to be Tested?
Is There a Treatment for HD?
What Kind of Care Does the Individual with HD Need?
What Community Resources are Available?
What Research is Being Done?
How Can I Help?
What is the Role of Voluntary Organizations?
Glossary
Information Resources
 
Huntington's Disease: Hope Through Research
National Institute of Neurological Disorders and Stroke
(NINDS 1998)
 
What Causes Huntington’s Disease?

HD results from genetically programmed degeneration of brain cells, called neurons, in certain areas of the brain. This degeneration causes uncontrolled movements, loss of intellectual faculties, and emotional disturbance. Specifically affected are cells of the basal ganglia, structures deep within the brain that have a number of important functions, including coordinating movement. Within the basal ganglia, HD especially targets neurons of the striatum, particularly those in the caudate nuclei and the pallidum. Also affected is the brain's outer surface, or cortex, which controls thought, perception, and memory.

 
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