Huntington's disease

Inherited brain disorder

Huntington's disease is an inherited neurological disorder causing progressive degeneration of brain cells.

Symptoms typically appear in middle age and include involuntary movements, cognitive decline, and psychiatric changes.

The disease is caused by a genetic mutation and is always fatal, usually within ten to twenty years of onset.

Also called Huntington's chorea, from the Greek for dance, describing the characteristic jerky movements.

symptoms

chorea

Involuntary jerking muscle disorder

cognitive decline · dementia · psychiatric symptoms · depression · irritability · apathy · involuntary movements · gait disturbance · dysphagia · dysarthria

inheritance

hereditary

Passed through generations

genetic counseling · risk factor · offspring · descendants · ancestry · bloodline · at-risk · presymptomatic · anticipation · late onset

genetics

dominant

Having superior influence

genotype · allele · penetrance · heritability · locus · DNA · gene · polymorphism · pathogenesis · genomics

treatment

antipsychotics

Drugs treating severe mental disorders

palliative care · clinical trials · supportive care · multidisciplinary · neurologist · psychiatrist · caregiver support

neurodegeneration

basal ganglia

Subcortical motor-control nuclei

white matter · gray matter · neuroimaging · MRI · PET scan · biomarkers

Categories
Opposites
genetic etiology

Huntington's diseaseinfectious disease

Pathogen-caused transmissible ailment

HIV/AIDS · tuberculosis · malaria · mesothelioma · traumatic brain injury

treatability/prognosis

Huntington's diseasebacterial infection

Illness from harmful microorganisms

strep throat · appendicitis · broken bone · benign tumor · vitamin deficiency

disease onset pattern

Huntington's diseasecongenital disorder

Condition present at birth

acute illness · stroke · heart attack · birth defect · Down syndrome

Family

disease, hunter, hunting, hunted, huntsman, huntress, Huntington, huntsmen, huntable

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