HUNTINGTON'S DISEASE

Huntington's disease is an inherited disease that causes the progressive breakdown of nerve cells in the brain. (Slowly shuts down the brain)

Huntington's disease is a dominant trait, and is autosomal. The genetics are composed of DNA a molecule shaped like a spiral ladder. Each is rung of this ladder

Each child of that person has a 25% chance if inheriting the condition.

SYMPTOMS
Movement Disorders:
Muscle cortacture.
Cognitive Disorders:
Difficulty focusing on tasks
Physiological Disorders:
Difficulty controlling emotions.

There is an estimate of 30,000 people in the world who have Huntington's disease.

The diagnosis of this disease is based primarily on your answers to questions.
1. Physical exam. 2. Family medical history. 3. Neurological examinations.

The average lifespan of someone with HD is 10-20 years. The younger the age, the more rapid the progression of the disease.

Medications can lessen some symptoms of movement and psychiatric disorder. There is no cure.

Everyday life for someone with this disease - Have to have social support and establish a daily routine. Any weight loss should be avoided. Self help groups will help cope with daily life.There are limitations.

Facts
- Psychiatric and Cognitive symptoms begin approximately 8-15 years before onset motor symptoms.

You would treat people with this disease like any other person.You would treat them with respect. And help them if they needed it.

WEBSITES:

• Www. Mayoclinic.org
• Caregiver.org
• Aoporphan.com

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THE END