1 of 10

Slide Notes

DownloadGo Live

Huntington's Disease

Published on Nov 20, 2015

No Description

PRESENTATION OUTLINE

SYMPTOMS

  • Usually develop at the ages of 30 to 50
  • Uncontrollable movement of arms, legs, head, face, and upper body
  • Decline in reasoning and thinking skills
  • Decline in memory, concentration,, judgement and ability
  • OCD

TREATMENT

  • There is no known cure
  • Dopamine blockers help reduce behaviors and movements
  • Amantadine and tetrabenazine control extra movements
  • There is also no known way to slow its progression

DISCOVERY

  • Discovered by Jonah Christian in 1860
  • First thorough description of it was by George Huntingtin
  • He found that it was genetically passed down

OTHER

  • Those who had it before it's naming
  • We're believed it be witches
  • And possessed by demons

LIFE EXPECTANCY

  • There is no way to tell how long someone will live with huntingtons
  • Patients can live anywhere from 10 to 30 years depending on the severity of symptoms

HOW IT WORKS

  • It is a neurodegenerative genetic, single gene disorder
  • Passed down from parent to child
  • Nerve cells degenerate
  • Affects muscle coordination
  • Mutation of gene in chromosome 4

Untitled Slide

WHAT IT AFFECTS

  • It affects your nerve cells
  • Muscle coordination
  • Brain cells become toxic to other cells

WHO IT EFFECTS

  • It affects parents who have it
  • Children of those who may have it
  • If a parent has Huntingtons there is a 50% chance of the child having it

DIAGNOSIS

  • A neurological exam
  • Neurologists, genetic counselors
  • Social workers, psychiatrists
  • and psychologists exam someone who
  • Are approved for the exam