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MOVEMENT DISORDER
SHREYA YADAV
NURSING TUTOR
SCHOOL OF NURSING
ST. CATHERINE’S
HOSPITAL
MOVEMENT DISORDERS
Movement disorders are neurologic conditions
that cause problems with movement, such as
Increased movement that can be voluntary
(intentional) or involuntary (unintended)
Decreased or slow voluntary movement.
DEFINITION
Movement disorders are clinical syndromes with
either an excess of movement or a paucity of
voluntary and involuntary movements,
unrelated to weakness or spasticity.
MOVEMENT DISORDERS
Ataxia.(Impaired balance or coordination,)
Dystonia(Repetitive muscle contractions)
Huntington's disease, (Chorea) Parkinson's
disease (Damaged Nerve cell ) Tourette
syndrome,
Tremor(shaking movements of body
parts.)
CAUSES
Genetics-
Infections
Damage to the brain, spinal cord,
or peripheral nerves
Metabolic disorders
Stroke and vascular diseases
Toxins.
HUNTINGTON'S
DISEASE(Chorea)
Huntington’s disease is a chronic,
progressive, hereditary disease of the
nervous system that results in progressive
involuntary choreiform movement and
dementia.
Huntington's disease is an inherited disease
that causes the progressive breakdown
(degeneration) of nerve cells in the brain.
FACTS
HD is named after George Huntington, the
physician who described it as hereditary
chorea in 1872.
Characteristic features of HD include
involuntary movements, dementia, and
behavioral changes.
CAUSES
The huntingtin gene defect involves extra
repeats of one specific chemical code in one
small section of chromosome 4. The normal
huntingtin gene includes 17 to 20 repetitions of
this code among its total of more than 3,100
codes.
The defect that causes Huntington's disease
includes 40 or more repeats. Genetic tests for
Huntington's disease measure the number of
repeats present in an individual's huntingtin
protein gene.
PATHOPHYSIOLOGY
Movement,Cognitive and mood symptoms
Excitotoxicity of neural cell due to High Ca2+
Excessive mutated glutamine proteinAggregated in neuronal cell of basal ganglia(Caudate and putamen)
Abnormally long polyglutamine sequence
Repetition of nucleotide triplets CAG (cytosine, adenine, and guanine)
Affects HTT (Huntingtin) on Chromosome -4
Due to (Genetic factor)
CLINICAL MANIFESTATION
Neurologic manifestation:
Involuntary jerking movements (chorea)
Muscle problems, such as rigidity or
muscle contracture (dystonia)
Slow or abnormal eye movements Impaired
gait, posture and balance
Difficulty with production of speech or
swallowing
COGNITIVE
MANIFESTATION
Difficulty organizing, prioritizing or focusing on
tasks
Lack of flexibility or the tendency to get stuck on a
thought, behavior or action .
Lack of awareness of one's own behaviors and
abilities
Slowness in processing thoughts or ''finding'' words
Difficulty in learning new information
PSYCHIATRIC MANIFESTATION
Most common - Depression
Feelings of irritability, sadness or apathy
Social withdrawal
Insomnia
Fatigue and loss of energy
DIAGNOSTIC EVALUATION
History:-
Physical examination:-
Neuropsychological testing
Genetic Testing
PET
CT and MRI
NON-PHARMACOLOGICAL MANAGEMENT
Nutritional therapy
Psychotherapy
Speech therapy
Physical therapy
Occupational therapy
PHARMACOLOGICAL MANAGEMENT
Tetrabenazine (reduces dopaminergic transmission).
Antidepressants include such drugs as citalopram (Celexa),
Antipsychotic drugs: such as quetiapine (Seroquel),
risperidone (Risperdal) may suppress violent outbursts,
agitation.
Anticonvulsants, such as valproate (Depacon), carbamazepine
(Carbatrol)
Nursing Management
Risk for injury from falls and possible skin
breakdown (pressure ulcers, abrasions), resulting
from constant movement.
Imbalanced nutrition, less than body requirements,
due to inadequate intake.
Anxiety and impaired communication from
excessive grimacing and unintelligible speech.
Disturbed thought processes and impaired social
interaction.

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MOVEMENT DISORDER GUIDE

  • 1. MOVEMENT DISORDER SHREYA YADAV NURSING TUTOR SCHOOL OF NURSING ST. CATHERINE’S HOSPITAL
  • 2. MOVEMENT DISORDERS Movement disorders are neurologic conditions that cause problems with movement, such as Increased movement that can be voluntary (intentional) or involuntary (unintended) Decreased or slow voluntary movement.
  • 3. DEFINITION Movement disorders are clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements, unrelated to weakness or spasticity.
  • 4. MOVEMENT DISORDERS Ataxia.(Impaired balance or coordination,) Dystonia(Repetitive muscle contractions) Huntington's disease, (Chorea) Parkinson's disease (Damaged Nerve cell ) Tourette syndrome, Tremor(shaking movements of body parts.)
  • 5. CAUSES Genetics- Infections Damage to the brain, spinal cord, or peripheral nerves Metabolic disorders Stroke and vascular diseases Toxins.
  • 6. HUNTINGTON'S DISEASE(Chorea) Huntington’s disease is a chronic, progressive, hereditary disease of the nervous system that results in progressive involuntary choreiform movement and dementia. Huntington's disease is an inherited disease that causes the progressive breakdown (degeneration) of nerve cells in the brain.
  • 7. FACTS HD is named after George Huntington, the physician who described it as hereditary chorea in 1872. Characteristic features of HD include involuntary movements, dementia, and behavioral changes.
  • 8. CAUSES The huntingtin gene defect involves extra repeats of one specific chemical code in one small section of chromosome 4. The normal huntingtin gene includes 17 to 20 repetitions of this code among its total of more than 3,100 codes. The defect that causes Huntington's disease includes 40 or more repeats. Genetic tests for Huntington's disease measure the number of repeats present in an individual's huntingtin protein gene.
  • 9. PATHOPHYSIOLOGY Movement,Cognitive and mood symptoms Excitotoxicity of neural cell due to High Ca2+ Excessive mutated glutamine proteinAggregated in neuronal cell of basal ganglia(Caudate and putamen) Abnormally long polyglutamine sequence Repetition of nucleotide triplets CAG (cytosine, adenine, and guanine) Affects HTT (Huntingtin) on Chromosome -4 Due to (Genetic factor)
  • 10.
  • 11.
  • 12. CLINICAL MANIFESTATION Neurologic manifestation: Involuntary jerking movements (chorea) Muscle problems, such as rigidity or muscle contracture (dystonia) Slow or abnormal eye movements Impaired gait, posture and balance Difficulty with production of speech or swallowing
  • 13. COGNITIVE MANIFESTATION Difficulty organizing, prioritizing or focusing on tasks Lack of flexibility or the tendency to get stuck on a thought, behavior or action . Lack of awareness of one's own behaviors and abilities Slowness in processing thoughts or ''finding'' words Difficulty in learning new information
  • 14. PSYCHIATRIC MANIFESTATION Most common - Depression Feelings of irritability, sadness or apathy Social withdrawal Insomnia Fatigue and loss of energy
  • 16. NON-PHARMACOLOGICAL MANAGEMENT Nutritional therapy Psychotherapy Speech therapy Physical therapy Occupational therapy
  • 17. PHARMACOLOGICAL MANAGEMENT Tetrabenazine (reduces dopaminergic transmission). Antidepressants include such drugs as citalopram (Celexa), Antipsychotic drugs: such as quetiapine (Seroquel), risperidone (Risperdal) may suppress violent outbursts, agitation. Anticonvulsants, such as valproate (Depacon), carbamazepine (Carbatrol)
  • 18. Nursing Management Risk for injury from falls and possible skin breakdown (pressure ulcers, abrasions), resulting from constant movement. Imbalanced nutrition, less than body requirements, due to inadequate intake. Anxiety and impaired communication from excessive grimacing and unintelligible speech. Disturbed thought processes and impaired social interaction.