Basal ganglia

The brain works together as one whole. Brain functions are spread throughout the brain areas and arise from the exchange between the areas. However, complaints can be identified per brain area.

 

The basal ganglia are also called the basal nuclei (nuclei basales) or deep nuclei

The word ganglion refers to a group of nerve cells with the same function. Ganglia is plural of ganglion.

 

The basal ganglia do not constitute an anatomical structure that can be easily identified. Although anatomically dispersed, they form a strong functional unit via many pathways. That is to say, this group of nuclei has similar functions. Some authors even consider nine nuclei to be part of the basal ganglia. The cerebellum and the basal ganglia together form what is also called the extrapyramidal system.

 

Functions

What do the basal ganglia do?

The basal ganglia help your brain make the right choices. They ensure that important actions proceed smoothly and that unnecessary actions are inhibited. In doing so, they work closely with the cerebrum (cerebral cortex), the thalamus and the cerebellum.

In summary, the basal ganglia have five important functions:

  • Regulating movement
    They help to start, execute, and stop movements smoothly. They also ensure that unwanted movements are suppressed.
    They regulate balance, posture, eye movements, and the initiation and planning of movements. They work together with brain areas that control movement and connect the thalamus to the motor cortex.

Directing eye movements
They help your eyes move quickly and accurately towards an object or person. This allows you to easily look from one point to another and shift your attention.

 

  • Learning automatic actions
    With a lot of practice, some actions become second nature. The basal ganglia play an important role in this. The basal ganglia regulate automatic movements, such as driving, cycling, knitting, maintaining balance, walking, typing, or driving. In adults, reflexes for posture are also stored here.

 

  • Supporting thinking and planning
    They assist in choosing an appropriate response, planning actions, switching between tasks, and making decisions.

 

  • Processing motivation and reward
    They play a role in motivation, experiencing rewards, and learning behaviors that yield success. As a result, they also influence initiative and perseverance.

 

  • Choosing the right behavior
    The basal ganglia help to select the most appropriate action from multiple possible options. At the same time, they inhibit actions that are less suitable at that moment.

 

Important to know

The basal ganglia do not directly control movements, eye movements, and behavior.
They function as a kind of control center that constantly assesses which movement, thought, or action best suits the situation. Subsequently, they send signals back via the thalamus to the cerebral cortex, where the final control takes place.

This cooperation makes it possible to move smoothly, act purposefully, and respond flexibly to changes. Therefore, damage to the basal ganglia can lead not only to movement problems but also to changes in thinking, motivation, emotions and behavior, motivation, reward, response to stimuli, addiction, and habit formation.

The basal ganglia can contribute to the neuropathology of depression, especially in relation to the limbic system. In schizophrenia, cognitive disorders, such as memory problems and learning difficulties, are linked to damage in this area.

 

 

Brief summary

  • The basal ganglia are also called basal nuclei or deep nuclei.
  • They function together and regulate:
    • balance, posture
    • planning of movements (including speech movements)
    • automatisms in movements
    • eye movements
    • motivation, reward/reinforcement of behavior and habit formation
    • emotions and regulation of emotions
    • learning simple processes
    • cognition (thinking functions) and language functions
  • In the event of disruption or injury, the above functions can change and a person can become depressed.

 

In-depth information for health care profesionals

Part 1. Parallel functional loops of the basal ganglia

Introduction

The basal ganglia do not constitute a separate anatomical organ, but rather a network of deep brain nuclei that functions via multiple parallel cortico-basal-ganglia-thalamo-cortical loops.

Each loop receives information from a specific area of ​​the cerebral cortex. This information is processed in the basal ganglia and sent back via the thalamus to virtually the same cortical area. As a result, various functions can be regulated largely independently of one another.

Although each loop has its own specialization, they all rely on the same principle:

The basal ganglia select the most suitable motor, oculomotor, cognitive, or behavioral program and suppress competing programs.

 

1. Motor loop


Main function
Selecting, refining, and regulating voluntary movements

Main cortical areas

  • Primary motor cortex
  • Premotor cortex
  • Supplementary motor cortex

Main nuclei

  • Putamen
  • GPe
  • GPi
  • Subthalamic nucleus
  • SNr

Via the thalamus

  • VA nucleus
  • VL nucleus

 

Clinical significance

Disorders primarily lead to hypokinesia, bradykinesia, rigidity, tremor, dystonia, chorea, or dyskinesias, depending on the affected circuit.

 

2. Oculomotor loop


Main function

Selecting and regulating voluntary eye movements, particularly saccades

Main cortical areas

  • Frontal Eye Fields
  • Supplementary Eye Field

 

Main nuclei

  • Caudate nucleus
  • SNr

Main connections

  • Superior colliculus
  • VA and MD thalamic nuclei

 

Clinical significance
Disorders may lead to delayed saccades, reduced visual exploration, and problems selecting relevant visual targets.

 

3. Dorsolateral prefrontal loop (associative loop)

 

Main function
Regulation of executive functions

 

Main cortical area

  • Dorsolateral prefrontal cortex

Main nuclei

  • Caudate nucleus
  • GPi
  • SNr

 

Via the thalamus

  • Mediodorsal (MD) nucleus
  • VA nucleus

Clinical significance
Disorders may lead to impaired planning, problems with working memory, reduced cognitive flexibility, slow thinking, and dysexecutive syndrome.

 

4. Lateral orbitofrontal loop


Main function
Regulation of behavioral inhibition and social decision-making


Main cortical area

  • Lateral orbitofrontal cortex

 

Main nuclei

  • Ventral striatum
  • GPi
  • SNr

 

Via the thalamus

  • Mediodorsal (MD) nucleus

 

Clinical significance

Disorders may lead to impulsivity, disinhibition, reduced insight into illness, and problems with social judgment.

 

5. Anterior cingulate (limbic) loop

 

Main function
Regulation of motivation, initiative, and reward-driven behavior

Main cortical area

  • Anterior cingulate cortex

 

Main nuclei

  • Nucleus accumbens
  • Ventral striatum
  • Ventral pallidum

 

Connections

  • Amygdala
  • Hippocampus
  • Ventral tegmental area (VTA)

 

Via the thalamus

  • Mediodorsal (MD) nucleus

 

Clinical significance
Disorders may lead to apathy, loss of initiative, anhedonia, and reduced goal-directed behavior.

Note: The ventral pallidum is functionally part of this loop but is not visible separately on the anatomical coronal atlas plate.

 

Summary

Although each loop has its own function, all loops use the same operating principle. The basal ganglia select the most appropriate program and inhibit competing programs.

How this happens is described in the next chapter.

 

Part 2 Mechanisms of action of the basal ganglia

 

Introduction

The selection of movements, eye movements, thoughts, and behavior takes place via three closely cooperating pathways:

  • the direct pathway
  • the indirect pathway
  • the hyperdirect pathway

These pathways are not separate loops, but form the common mechanisms of action within the various functional circuits.

 

The direct pathway

Main function
Facilitates the execution of the selected program.

 

Simplified circuit
Cortex → Striatum → GPi/SNr → Thalamus → Cortex

 

Principle of operation
The striatum inhibits GPi and SNr.

This reduces the inhibition of the thalamus (disinhibition), allowing the thalamus to activate the cerebral cortex more strongly.

Consequently, the selected program is given a greater chance of being executed.

 

Net effect

  • Facilitates desired movements.
  • Facilitates desired eye movements.
  • Facilitates desired cognitive processes.
  • Facilitates goal-directed behavior.

 

The indirect pathway

Main function

Suppresses competing programs.

 

Simplified circuit
Cortex → Striatum → GPe → Subthalamic nucleus → GPi/SNr → Thalamus → Cortex

 

Mode of action
Via GPe and the subthalamic nucleus, the activity of GPi and SNr increases.

This strengthens the inhibition of the thalamus, giving competing programs less chance to be executed.

Net effect

  • Inhibits unwanted movements.
  • Inhibits unwanted eye movements.
  • Inhibits competing cognitive processes.
  • Inhibits unwanted behavior.

 

The hyperdirect pathway

Main function

Ensures very rapid, temporary inhibition.

Simplified circuit
Cortex → Subthalamic nucleus → GPi/SNr → Thalamus → Cortex

 

Principle of operation
The cerebral cortex directly activates the subthalamic nucleus. As a result, the activity of GPi and SNr increases almost immediately, causing the thalamus to be powerfully inhibited.

This makes it possible to interrupt an ongoing program immediately.

 

Net effect

  • Rapid stop function
  • Rapid response inhibition
  • Ability to interrupt an action or behavior immediately

 

Dopaminergic Modulation

The substantia nigra pars compacta (SNc) modulates the striatum with dopamine.

  • Dopamine stimulates the direct pathway via D1 receptors.
  • Dopamine reduces the activity of the indirect pathway via D2 receptors.

This promotes the execution of desired programs while preventing excessive inhibition.

 

Clinical Significance
Normally, the direct, indirect, and hyperdirect pathways maintain a balance.

Disruption of this balance leads to motor, oculomotor, cognitive, and behavioral disorders.

The nature of the symptoms depends on which pathway and which functional loop are most affected.

 

Anatomical References

  • Gray's Anatomy: The Anatomical Basis of Clinical Practice
  • Mai JK, Paxinos G. The Human Nervous System
  • Blumenfeld H. Neuroanatomy Through Clinical Cases
  • Alexander GE, DeLong MR, Strick PL. Parallel Organization of Functionally Segregated Circuits Linking Basal Ganglia and Cortex. Annual Review of Neuroscience. 1986.

© Hersenletsel-uitleg.nl No part of this text may be reproduced without permission from the authors.

Where in the brain?

The basal ganglia as a functional unit

The basal ganglia consist of multiple deep brain nuclei that work together as a single functional unit via extensive nerve connections.

In the image above, the following parts are numbered:

1. Caudate nucleus / Nucleus caudatus (tail nucleus)
Together with the putamen, the caudate nucleus forms the
dorsal striatum.

2. Putamen (shell)
Together with the caudate nucleus, the putamen forms the
dorsal striatum.

5. Nucleus accumbens (accumbens nucleus)
The nucleus accumbens forms the ventral transition between the caudate nucleus and the putamen and belongs to the ventral striatum.

Note: The olfactory tubercle (tuberculum olfactorium) also belongs to the ventral striatum, but is not depicted in this coronal section.

3. Globus pallidus externus (GPe)

4. Globus pallidus internus (GPi)

Together, GPe and GPi form the Globus pallidus (pale globe).

6. Subthalamic nucleus / Nucleus subthalamicus 

7. Black nucleus (substantia nigra pars compacta) (SNc)

8. Black nucleus (substantia nigra pars reticulata) (SNr)

Together, SNc and SNr form the substantia nigra (black nucleus)

 

Important to know

  • The basal ganglia consist of multiple deep brain nuclei.
  • Dorsal striatum: caudate nucleus + putamen
  • Ventral striatum: nucleus accumbens + olfactory tubercle
  • Lentiform nucleus (nucleus lentiformis): putamen + globus pallidus (GPe and GPi)
  • The olfactory tubercle is anatomically part of the ventral striatum, but is not visible in this cross-section.
  • The basal ganglia do not form a continuous anatomical structure, but a functional network of anatomically separated nuclei.

 

Lateral view of the basal ganglia structures:

 

Picture info see footnotes Lim Fiez Holt

 

The picture above is a cross section of the brain showing basal ganglia.

On the picture below you see the tegmentum. The tegmentum is part of the midbrain, the upper part of the brainstem.
There is the substantia nigra located.

Anatomy and function of the subregions of the basal ganglia

Corpus striatum

The corpus striatum literally means 'the striped body' and can be divided into:

1. Striatum dorsale (dorsal side) with two parts:

Putamen

The putamen is involved, among other things, in the regulation of motor skills, both voluntary and involuntary movements.

It helps the limbs prepare for movement and helps with movement. Furthermore, the putamen is involved in learning and motor control of speech, such as speech articulation. Damage to the putamen may lead to problems such as speech apraxia and dysarthria.

The putamen is also necessary for language functions, reward, cognitive functioning and addiction.

A wide spectrum of movement disorders, cognitive and psychiatric disorders can result from injury in the putamen.
It can result in involuntary, jerky muscle movements or tremors such as in Huntington's disease. Parkinson's disease is the result of dopamine deficiency in the posterior putamen and is characterized by stiffness, tremors, ataxia and disturbance of balance.

Restless legs syndrome can also be a result of injury to the putamen. Restless legs syndrome causes jerking of the legs and a painful urge to move the legs.


Furthermore, the following diseases are associated with damage to the putamen: Alzheimer's disease, Lewy body dementia, obsessive compulsive disorder (OCD), bipolar disorder, Tourette syndrome, and ADHD; attention deficit hyperactivity disorder. A decrease in putamen volume is seen in major depressive disorder, Williams syndrome, autism and schizophrenia.


The putamen and the globus pallidus together form, anatomically (not in terms of function), the lens nucleus or the lentiform or lenticular nucleus.

 

Image of the putamen:

 

Nucleus Caudate

Nucleus caudate / caudate nucleus (tail nucleus) has the shape of an elongated C in both hemispheres. It plays an important role in our emotional and social life.

This area works together with other brain structures to process rewards, such as positive emotions we feel from mutual affection or a close connection with others.

Additionally, the caudate nucleus plays a role in strengthening social bonds by linking positive experiences to specific people or situations.

It has the following functions:

  • motivation and reward, including the desire for reward

  • transmitting information about the position of your body

  • maintaining proper posture of your body, arms, and legs

  • ensuring that your movements are precise

  • determining how fast you move

  • storing memories, short and long

  • understanding language

  • learning new things

  • processing feedback

 

The information travels via the putamen and globus pallidus to the
thalamus, and subsequently reaches the frontal cortex.
Recent research has shown that something changes in the caudate nucleus, which may explain the fatigue associated with Multiple Sclerosis and traumatic brain injury.

 

Image of the nucleus caudate / caudate nucleus

 

 

The striatum ventrale (on the ventral side)

This ventral part is considered part of the limbic system.

  • Nucleus accumbens is part of the reward system in the brain and plays a role in behavior.

    It helps with pain management through the release of dopamine and serotonin, which play a role in pain and pleasure.

    You can find more explanation about this on the page about pain and brain regions.

 

  • Olfactory tubercle (tuberculum olfactorium) is part of the olfactory tract for odor perception.

 

Certain parts of the caudate nucleus and the putamen are also included in the striatum ventrale.

 

 

Globus pallidus or Pallidium


The globus pallidus, also known as the pale sphere, is divided into two segments: the internal segment (globus pallidus internus) and the external segment (globus pallidus externus). The two segments work together with other brain regions to enable smooth and precise movements.

 

Function
The globus pallidus helps regulate movements and plays a role in learning. It uses dopamine for this purpose, a substance produced in the substantia nigra (black nucleus). It transmits information from the basal ganglia to the thalamus via GABA, a substance that inhibits movements.

 

Causes of damage
The globus pallidus may be damaged by carbon monoxide poisoning, oxygen deficiency (hypoxia), poisoning with the strong sleeping and sedative barbiturate (barbiturate intoxication), cyanide poisoning, hydrogen sulfide poisoning, severe prolonged low blood sugar levels (hypoglycemia), low blood pressure (hypotension), and copper accumulation in the body: Wilson's disease.

 

Consequences of damage
Damage to the globus pallidus affects learning functions and movement disorders.
Pallidus or pallidum literally means the pale inner region (see also the next paragraph).

 

Image of the Globus pallidus

 

Lentiform or lenticular nucleus (lens nucleus)

The putamen and the globus pallidus together form the lens nucleus or the lentiform or lenticular nucleus. It gets its name from its shape of a lens.
The globus pallidus forms the conical part of the lentiform nucleus for which the putamen forms a cap.
There is no functional unit, only an anatomical connection. They are separated by a thin layer of white matter: the medial medullary lamina.

 

Function

The lens nucleus is important for learning, motivation, and motor skills.

It is sometimes associated with aggression when damaged.

The lens nucleus is described in various conditions, such as atypical Parkinson's syndromes (MSA, PSP), Wilson's disease (copper accumulation) and dystonia.

 

 

Subthalamic nucleus

The subthalamic nucleus or subthalamic nucleus (Luys' bodies) includes:

  • Dorsal (motor) part, which receives input from the primary motor cortex.
  • Ventrolateral (associative) part, which receives input from the prefrontal cortex and frontal eye fields.
  • Ventromedial (limbic) part, which receives input from the anterior cingulate cortex.

The subthalamic nucleus is involved in voluntary and involuntary movements, associative learning and limbic functions.
For the movement disorders that can occur due to damage to the subthalamic nucleus, see the bottom of this page.

Black core / Substantia nigra

The black nucleus or substantia nigra is located in the front part of the mesencephalon (midbrain) and supplies the basal ganglia with dopamine. It is a motor nucleus. Despite its location in the mesencephalon, it is considered part of basal ganglia in function. The black nucleus is involved in voluntary movements, orientation in space, learning, mood regulation, and activity related to the reward circuit of the brain.

 

It consists of:

  • The pars compacta (SNc) on the dorsal side with melanin-filled neurons. Melanin is the dark color (pigment) that gives the black core its name. It supplies the striatum with dopamine and is very important for transmitting signals from the basal ganglia to the thalamus. It is involved in motor control and coordination. From the substantia nigra, nerve pathways run to the striatum (striped body). This is called the nigrostriatal pathway.
    The loss of dopamine neurons in this part (SNc) appears to be responsible for the development of Parkinson's disease and some other parkinsonian syndromes.
    Dopamine is a signaling substance (neurotransmitter) that is related to movement disorders, psychiatric disorders and behavioral problems.
    Read more about dopamine via this link.
  • The pars reticulata (SNr) on the ventral side is important in the regulation of eye movements.

 

Injury to parts of the basal ganglia

Damage to the basal ganglia can be caused by various types of brain injury, including cerebral hemorrhage, cerebral infarction, tumor or silent cerebral infarction (SCI) that goes unnoticed except during an accidental brain scan.

 

Movement disorders

The consequences of damage to the basal ganglia can be the following movement disorders:

  • Ataxia is a balance and coordination disorder, a movement disorder. Balance and coordination of movement are affected.
    A person with ataxia has an uncertain gait and moves his arms, legs and torso in a 'jerky' and uncontrolled manner.

 

  • Athetosis is characterized by continuous, slow, involuntary movements of fingers, hands, feet and toes, sometimes arms, legs, neck and tongue. The fingers are often overextended. The joints writhe or contort continuously or while rolling slowly. When the facial muscles move, the face appears to be grimacing. The neck muscles appear thickened (hypertrophy) because the neck muscles contract frequently and the head then turns.

 

  • Ballism (proximal chorea) is characterized by involuntary, lurching irregular, coarse movements. It is related to chorea but the movements in ballism are slower than in chorea. Ballism often involves, as the name 'proximal chorea' indicates, proximal body parts. Proximal means closer to the center of the body than any other part of the body. In the case of ballism, it concerns the hip, thighs, upper arms and shoulders. The hip joint is located proximal to the knee joint. The upper arms lie proximal to the forearms.
    Ballism is often caused by damage to the subthalamic nucleus, which is part of the basal ganglia.
    Globus pallidus, Putamen or Caudate nucleus, the other parts of the basal ganglia, can also be disturbed.
    During sleep the movements may calm down, but when aroused, the movements become stronger. Causes of ballism can be: bleeding, an infarction, a tumor or metastasis (spread) or an infection.
    If it occurs on one side of the body, it is called hemiballism.
    The term 'Ballism' is derived from the Greek word for throwing and swinging. Ballism is one of the hyperkinetic movement disorders. The term 'hyperkinetic' means: with excessive energy.

See the video under hemiballism. Hemiballism is ballism on one side of the body.

 

  • Bradykinesia is characterized by a general slowness of movement and is the most common form of reduced movement
    (hypokinesia). For example, a person may move back and forth in the chair a few times before he or she can get up. Automatic movements, such as blinking the eyes, are less fast and smooth. This occurs, for example, in Parkinson's disease, other conditions and due to old age.

 

  • Chorea is characterized by sudden, irregular, involuntary, undirected (purposeless), continuous, 'dance-like', sometimes graceful movements of the face, hands, arms, neck or torso. The movements may last for several seconds to minutes and are not rhythmic in nature. The movements cannot be suppressed and there is no urge to move. 'Chorea' is the Greek word for dance. It is caused by injury in the Red Nucleus or by injury in the basal ganglia. There are several diseases in which chorea occurs, but the most characteristic is Huntington's disease. This involves degeneration of striatal GABA neurons, causing the head of the Caudate nucleus to become smaller (atrophy).

 

  • Dystonia is characterized by involuntary, persistent muscle contractions; spasms in muscles or muscle groups.

This can cause repetitive or twisting movements or an unnatural position of the body part. The often painful movements are often accompanied by a tremor.
Forms of dystonia can be classified by cause, age of onset, or by distribution over the body.
It may involve single muscle groups (focal dystonia), for example in spasmodic torticollis, or multiple muscle groups (generalized dystonia: extensive dystonia). Then one or both legs, the trunk and at least one other body part are involved.
In spasmodic torticollis (Cervical dystonia) there is a dystonia of the neck and neck muscles. If the head is crooked, it is called laterocollis. When the neck is turned to one side, this is called rotational torticollis. When the head is turned backwards, this is called retrocollis.
The eyelids may remain closed in a cramp. That's called blepharospasm; literally 'eyelid contraction'.
Furthermore, further divisions can be made into segmental (dystonia concerns two adjacent body parts), hemidystonia (dystonia concerns one half of the body, usually due to brain damage) and multifocal (in a number of body parts that are not adjacent to each other).
Symptoms of dystonia may include:

  • Abnormal posture of the neck, toes, hands or other parts of the body.
  • Involuntary turning of the neck when tired or  stressed.
  • Uncontrollably rapid blinking of the eyes.
  • Spasms of the eyelids causing the eyelids to remain closed.
  • Cramp in the foot or the tendency of a foot to turn over after walking.
  • Problems with writing that cause handwriting to deteriorate after writing a few lines.

 

Dystonia is one of the conditions that can follow damage to the basal ganglia.
Dystonia can also have a genetic cause.

More information on dystonia can be found on Dystonia UK and on Dystonia Medical Research Foundation. 

 

  • Hemiballism is characterized by wild, involuntary, lurching, coarse movements of the limbs on one side of the body.

It is related to chorea but in ballism the movements are slower than in chorea. Ballism is often caused by damage to the subthalamic nucleus, which is part of the basal ganglia.
The Globus pallidus, Putamen, Caudate nucleus, other parts of the basal ganglia can also be disturbed.
During sleep the movements may calm down, but when aroused the movements become stronger. Causes of ballism include: bleeding, an infarction, a tumor or metastasis or an infection.
See more information above under Ballism.

 

  • Hemiballismus-hemichorea (HBHC) syndrome is a rare hyperkinetic movement disorder.

Characteristic are involuntary, irregular, continuous, unilateral movements of the body. It is caused by damage to the basal ganglia due to a cerebral infarction, cerebral hemorrhage,
autoimmune diseases. Although rare, high blood sugar (hyperglycemia) is another possible cause of HBHC syndrome, also known as chorea-hyperglycemia-basal ganglia syndrome.
The diagnosis can be made if there are three abnormalities: chorea, high blood sugar (hyperglycemia) and radiological abnormalities
in a specific part of the basal ganglia, namely the striatum.

 

  • Hemichorea is chorea on one side of the body. See above under Chorea.

 

  • Hyperkinetic movement disorders are characterized by excessive and involuntary increased muscle activity, such as in Huntington's disease. They are involuntary excessive normal and abnormal movements. Sometimes accompanied by athetosis, ballism, trembling and/or chorea.

 

  • Myoclonus is a short-lived, jerky, involuntary and usually arrhythmic (sometimes rhythmic) movement, with the same movement over and over. There is no urge to move. A myoclonus cannot be suppressed. The word 'myoclonus' comes from the words 'myo' meaning muscle and 'clonus' meaning shock. It can occur as an innocent muscle contraction, but also in epilepsy syndromes in addition to absence seizures and tonic-clonic seizures. They are called subcortical myoclonies if they occur through subcortical (located below the cerebral cortex) areas of the brain, such as the basal ganglia.

Myoclonias may be caused by genetic disorders, metabolic diseases, brain disorders (encephalopathy) caused by poorly functioning kidneys, liver, thyroid or by COVID-19. Myoclonias may also be caused by brain injury, for example: traumatic brain injury, brain inflammation/encephalitis, autoimmune inflammation of the brain, cerebral infarction/ischemic stroke and oxygen deficiency (hypoxic-ischaemic encephalopathy/HIE). Finally, myoclonias can be caused by medications. Myoclonias can also occur alongside other movement disorders, such as ataxia, dystonia or chorea.

 

  • Tremors are characterized by abnormal involuntary, rhythmic movements of the hand, head or other body parts.

 

  • Tics are sudden, brief, rapid and recurrent, non-rhythmic and stereotypic semi-voluntary motor movements lasting seconds. There is an urge to move. Tics always occur in the same movement. There may be multiple tics. The tics can be suppressed for a short time and are therefore called semi-voluntary movements. In particular the Striatum, part of the basal ganglia, plays a role.
    In the condition PANDAS, children develop tics after experiencing a streptococcal infection (for example, after a throat infection or wound).
    The tics are then accompanied by behavioral disturbances. Tics can also be caused by medications. This website has extensive information on PANDAS.

 

Parkinsonism

The combination of postural problems associated with damage to the basal ganglia is called parkinsonism because they are reminiscent of Parkinson's disease.

  • changed movement pattern, slowed movement
  • difficulty speaking, word-finding problems
  • difficulty with posture and movements
  • tremors; shaking, shaking and trembling
  • involuntary movements, spasms
  • increased muscle tension, muscle stiffness
  • abnormal body position
  • difficulty with balance and difficulty walking
  • difficulty seeing due to inability to control eye movement
  • difficulty starting a movement, keeping it going and stopping a movement
  • uncontrolled repetitive movements such as in tics, also in uttering cries.

There are many diseases that resemble the symptoms of Parkinson's disease. The conditions that resemble Parkinson's disease are called atypical parkinsonisms.
Atypic parkinsonisms include vascular parkinsonism and multiple system atrophy (MSA) and progressive supranuclear palsy (PSP).
Spasticity is not one of the consequences of damage to the basal ganglia. Read about spasms and spasticity.

 

The following conditions and conditions involve the basal ganglia:

 

 

Disorders Of The Basal Ganglia 1

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