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MYOCLONIC EPILEPSY

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Sometimes these little jerks are followed by tonic-clonic or absence seizures. ... PME is a combination of myoclonic and tonic-clonic seizures. ... – PowerPoint PPT presentation

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Title: MYOCLONIC EPILEPSY


1
MYOCLONIC EPILEPSY
  • BY TRYSHA SRONCE

2
WHAT IS MYOCLONIC EPILEPSY?
  • Epilepsy is a disorder of the central nervous
    system.
  • When a person has epilepsy, the brains
    electrical rhythms become imbalanced and cause
    recurrent seizures.
  • Myoclonic epilepsy is usually quick little jerks
    of the arms, shoulders, and occasionally the
    legs.
  • Myoclonus is the brief, involuntary twitching of
    a muscle or group of muscles.

3
WHAT CAUSES MYOCLONIC EPILEPSY?
  • Exactly what causes epilepsy is unknown for about
    half the people it effects.
  • Myoclonic twitches are usually caused by sudden
    muscles contractions.
  • Myoclonus may develop in response to infection,
    head or spinal cord injury, stroke, brain tumors,
    and many other diseases.
  • Myoclonus can occur by itself, but most often it
    is one of several symptoms associated with a wide
    variety of nervous system disorders.

4
SYMPTOMS
  • Myoclonic seizures are often described as
    jumps. These jumps are caused by the rapid
    contraction and relaxation of the muscles.
  • Seizures affect different people in different
    ways and they can take many forms. Many seizures
    have a beginning, middle, and end.
  • BEGINNING not everyone is aware of a beginning.
    Some seizures will come without warning. A person
    may sense an aura about them just before a
    seizure.

5
SYMPTOMS
  • MIDDLE people that experience warnings might see
    the aura just continue or it can turn into a
    complex partial seizure or convulsion. People
    without warnings might just jump into the partial
    seizure.
  • END the post-ictal period is the recovery
    period of the brain back to its normal state. The
    length of a recovery time can depend on what area
    of the brain was affected and whether or not the
    person was on any anti-seizure medications. The
    post-ictal period can last anywhere from seconds
    to hours.

6
SYMPTOMS OR WARNINGS
  • EARLY WARNING SIGNS
  • Déjà vu, smells, sounds, tastes, vision lost,
    racing thoughts, fear, panic, pleasant feelings,
    dizziness, lightheaded, nausea, and numbness.
  • SEIZURE SYMPTOMS
  • Blackout, confusion, deafness, loss of
    consciousness, convulsions, stiffening,
    difficulty breathing, incontinence, inability to
    move.
  • AFTER SEIZURE SYMPTOMS
  • Memory loss, confusion, frustration, headache,
    nausea, pain, exhaustion, fear, thirst, and
    difficulty speaking.

7
TREATMENT AND PROGNOSIS
  • The exact origins of myoclonus are unclear so it
    may require multiple drugs that work on different
    brain pathways for effective treatment.
  • The downside to these drugs is that many of the
    side effects become harmful if taken for long
    periods of time.
  • Patients often develop tolerance for the drugs so
    they need to be monitored closely.
  • PROGNOSIS
  • Myoclonus is not a life threatening disorder but
    it can result in very serious, debilitating
    impairments.

8
2 MAIN TYPES OF MYOCLONIC EPILEPSY
  • JUVENILE MYOCLONIC EPILEPSY (JME)
  • People afflicted with JME have myoclonic
    seizures, usually in the morning soon after they
    wake up.
  • Sometimes these little jerks are followed by
    tonic-clonic or absence seizures.
  • JME patients have seizures that are triggered by
    flickering lights on T.V., games, or at dances as
    well as light reflecting off water.
  • More than 80 of the JME population find that
    their seizures are controlled very well by
    medication.

9
2 MAIN TYPES OF MYOCLONIC EPILEPSY
  • PROGRESSIVE MYOCLONIC EPILEPSY (PME)
  • PME is a combination of myoclonic and
    tonic-clonic seizures.
  • Some additional symptoms are muscles rigidity,
    unsteadiness, and mental deterioration.
  • PME is a group of rare disorders that strike at
    any age depending on the type of myoclonic
    epilepsy a person has. Some PME syndromes
    include
  • Severe myoclonic epilepsy of infancy (Dravet
    Syndrome)
  • Unverrich-Lundberg Disease
  • Lafora Disease
  • Mitochondrial Encephalopathies

10
TREATMENTS OF PME
  • Treatments of PME are usually only successful for
    a few months or years. As the disorder
    progresses, the anti-seizure medications become
    less effective.
  • This makes the outlook generally unfavorable.
  • Patients often lose their abilities to think and
    move, but results vary on a case by case basis.

11
QUESTIONS???
  • 1.) Myclonus may develop in response to ______.
  • A. Infection B. Brain tumors
  • C. Stroke D. All of the above
  • 2.) Epilepsy is a disorder of the ______.
  • A. Central Nervous System
  • B. Peripheral Nervous System
  • 3.) Patients often develop ______ the drugs they
    take during treatment.
  • A. an addiction to B. a tolerance for
  • C. tumors from D. random seizures from
  • 4.) People with Juvenile Myoclonic Epilepsy
    usually have seizures in the ____.
  • A. morning B. afternoon
  • C. night D. 500 p.m.
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