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Introduction
1. Anatomy
2. Microbiology
3. Physiology
4. Pathology
4.1 General pathology
4.2 Central and peripheral nervous system
4.2.1 Cerebrovascular disorders
4.2.2 Pathophysiology
4.2.3 Trauma to the CNS
4.2.4 Increased intracranial pressure
4.2.5 Neurodegenerative disorders and dementia
4.2.6 Seizure disorders
4.2.7 Disorders associated with headache
4.2.8 Neuropathies
4.2.9 Sleep disorders
4.2.10 Movement disorders
4.2.11 Metabolic and demyelinating disorders
4.2.12 Neoplasms
4.2.13 Congenital disorders
4.2.14 Spinal cord disorders
4.2.15 Additional information
4.3 Cardiovascular system
4.4 Respiratory system
4.5 Hematology and oncology
4.6 Gastrointestinal pathology
4.7 Renal, endocrine and reproductive system
4.8 Musculoskeletal system
5. Pharmacology
6. Immunology
7. Biochemistry
8. Cell and molecular biology
9. Biostatistics and epidemiology
10. Genetics
11. Behavioral science
Wrapping up
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4.2.10 Movement disorders
Achievable USMLE/1
4. Pathology
4.2. Central and peripheral nervous system

Movement disorders

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(I) Tourette syndrome (TS): Tourette syndrome is a neurological disorder characterized by repetitive, stereotyped, involuntary movements and vocalizations called tics that are present for at least a year. It typically begins between the ages of 3-9 years and is more common in males.

Tics are classified as either simple or complex.

Simple motor tics are sudden, brief, repetitive movements that involve a limited number of muscle groups. Common simple motor tics include eye blinking and other eye movements, facial grimacing, shoulder shrugging, and head or shoulder jerking.

Simple vocalizations might include repetitive throat-clearing, sniffing, or grunting sounds.

Complex tics are distinct, coordinated patterns of movements involving several muscle groups. Complex motor tics might include facial grimacing combined with a head twist and a shoulder shrug. Other complex motor tics may appear purposeful, including sniffing or touching objects, hopping, jumping, bending, or twisting.

Coprolalia (uttering socially inappropriate words such as swearing) or echolalia (repeating the words or phrases of others) are seen.

Abnormalities in certain brain regions, including the basal ganglia, frontal lobes, cortex, and hypertrophy of the thalamus, have been demonstrated. Low serotonin in the brainstem, low levels of glutamate in the globus pallidus, and low levels of cAMP in the cortex are seen. An increase in the density of the presynaptic dopamine transporter and the postsynaptic D2 dopamine receptor, suggesting increased dopamine activity, has been postulated.

ADHD, depression, anxiety, and OCD may be associated with TS.

(II) Adult onset tic disorders: Onset of tic disorders in adulthood, typically after the age of 21 years, is called adult onset tic disorder. Most cases are secondary to neurodegenerative disorders like Huntington’s disease, brain trauma, cocaine abuse, viral encephalitis, medication side effects, etc.

(III) Essential tremor: It is characterized by involuntary, rhythmic movements of the hands or arms, or less commonly involving the neck, jaw, or tongue. It can be fast or slow. It becomes worse with movement, stress, fatigue, caffeine, and hypoglycemia. It may be inherited in an autosomal dominant fashion.

People with essential tremor are at increased risk of developing Alzheimer’s disease and Parkinson’s syndrome. Essential tremors may briefly subside after the ingestion of alcohol.

Tourette syndrome (TS)

  • Neurological disorder with repetitive, involuntary tics (motor and vocal) for ≥1 year
  • Onset: ages 3–9, more common in males
  • Tics:
    • Simple: brief, repetitive (e.g., eye blinking, throat-clearing)
    • Complex: coordinated, purposeful-appearing (e.g., hopping, touching objects)
    • Coprolalia and echolalia may occur
  • Brain abnormalities: basal ganglia, frontal lobes, cortex, thalamus; neurotransmitter changes (↓serotonin, ↓glutamate, ↓cAMP, ↑dopamine activity)
  • Associated with ADHD, depression, anxiety, OCD

Adult onset tic disorders

  • Onset after age 21
  • Usually secondary to other conditions:
    • Neurodegenerative diseases (e.g., Huntington’s)
    • Brain trauma, substance abuse, encephalitis, medication side effects

Essential tremor

  • Involuntary, rhythmic hand/arm movements; may affect neck, jaw, tongue
  • Worsens with movement, stress, fatigue, caffeine, hypoglycemia
  • May be autosomal dominant (inherited)
  • Increased risk of Alzheimer’s and Parkinson’s
  • Tremor may temporarily improve with alcohol

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Movement disorders

(I) Tourette syndrome (TS): Tourette syndrome is a neurological disorder characterized by repetitive, stereotyped, involuntary movements and vocalizations called tics that are present for at least a year. It typically begins between the ages of 3-9 years and is more common in males.

Tics are classified as either simple or complex.

Simple motor tics are sudden, brief, repetitive movements that involve a limited number of muscle groups. Common simple motor tics include eye blinking and other eye movements, facial grimacing, shoulder shrugging, and head or shoulder jerking.

Simple vocalizations might include repetitive throat-clearing, sniffing, or grunting sounds.

Complex tics are distinct, coordinated patterns of movements involving several muscle groups. Complex motor tics might include facial grimacing combined with a head twist and a shoulder shrug. Other complex motor tics may appear purposeful, including sniffing or touching objects, hopping, jumping, bending, or twisting.

Coprolalia (uttering socially inappropriate words such as swearing) or echolalia (repeating the words or phrases of others) are seen.

Abnormalities in certain brain regions, including the basal ganglia, frontal lobes, cortex, and hypertrophy of the thalamus, have been demonstrated. Low serotonin in the brainstem, low levels of glutamate in the globus pallidus, and low levels of cAMP in the cortex are seen. An increase in the density of the presynaptic dopamine transporter and the postsynaptic D2 dopamine receptor, suggesting increased dopamine activity, has been postulated.

ADHD, depression, anxiety, and OCD may be associated with TS.

(II) Adult onset tic disorders: Onset of tic disorders in adulthood, typically after the age of 21 years, is called adult onset tic disorder. Most cases are secondary to neurodegenerative disorders like Huntington’s disease, brain trauma, cocaine abuse, viral encephalitis, medication side effects, etc.

(III) Essential tremor: It is characterized by involuntary, rhythmic movements of the hands or arms, or less commonly involving the neck, jaw, or tongue. It can be fast or slow. It becomes worse with movement, stress, fatigue, caffeine, and hypoglycemia. It may be inherited in an autosomal dominant fashion.

People with essential tremor are at increased risk of developing Alzheimer’s disease and Parkinson’s syndrome. Essential tremors may briefly subside after the ingestion of alcohol.

Key points

Tourette syndrome (TS)

  • Neurological disorder with repetitive, involuntary tics (motor and vocal) for ≥1 year
  • Onset: ages 3–9, more common in males
  • Tics:
    • Simple: brief, repetitive (e.g., eye blinking, throat-clearing)
    • Complex: coordinated, purposeful-appearing (e.g., hopping, touching objects)
    • Coprolalia and echolalia may occur
  • Brain abnormalities: basal ganglia, frontal lobes, cortex, thalamus; neurotransmitter changes (↓serotonin, ↓glutamate, ↓cAMP, ↑dopamine activity)
  • Associated with ADHD, depression, anxiety, OCD

Adult onset tic disorders

  • Onset after age 21
  • Usually secondary to other conditions:
    • Neurodegenerative diseases (e.g., Huntington’s)
    • Brain trauma, substance abuse, encephalitis, medication side effects

Essential tremor

  • Involuntary, rhythmic hand/arm movements; may affect neck, jaw, tongue
  • Worsens with movement, stress, fatigue, caffeine, hypoglycemia
  • May be autosomal dominant (inherited)
  • Increased risk of Alzheimer’s and Parkinson’s
  • Tremor may temporarily improve with alcohol