Basal ganglion disease: Difference between revisions
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=== Clinic === | === Clinic === | ||
* There are three form of basal Ganglia diseases: | |||
# [[Hyperkinetic movement disorders|Hyperkinetic disorders]]: Failing to properly suppress unwanted movements | |||
# Hyperkinetic disorders: Failing to properly suppress unwanted movements | |||
# Hypokinetic disorders: Failing to properly prime upper motor neuron circuits to initiate motor function. | # Hypokinetic disorders: Failing to properly prime upper motor neuron circuits to initiate motor function. | ||
# Undefined form | # Undefined form | ||
=== [[Hyperkinetic movement disorders|Hyperkinetic disorders]] === | |||
* Huntington's disease | |||
* [[Dystonia miasms|Dystonia]]: It can occur as a Hyperkinetic or Hypokinetic disorder or as a side effect of disorders such as Parkinson's disease. | |||
=== | * [[Chorea|Hemiballismus]]: It is a hyperkinetic movement disorder that causes uncontrolled movement on one side of the body. | ||
* | |||
=== | === Hypokinetic disorders === | ||
* [[Parkinsonism]]: [[Rigidity]] + Rest [[tremor]] + Bradykinesia (Slowness in initiation and execution of movement) | |||
=== | === Undefined form === | ||
The following diseases that generally involve the basal ganglia do not clearly fit into being either hypo- or hyperkinetic. | The following diseases that generally involve the basal ganglia do not clearly fit into being either hypo- or hyperkinetic. | ||
* Epilepsy | * [[Seizure|Epilepsy]] | ||
* [[ | * [[Tourette syndrome]] / [[Obsessive-Compulsive Disorder (OCD)|Obsessive–compulsive disorder]]: | ||
* [[Sydenham's chorea entities|Sydenham's chorea]]: | * [[Sydenham's chorea entities|Sydenham's chorea]]: Characterized by rapid, uncoordinated jerking movements primarily affecting Face / Hands / Feet. It is a result of an autoimmune response that occurs following infection by [[GABHS, Group A beta hemolytic streptococcus|GABHS]] that destroys cells in the corpus striatum. | ||
* [[PANDAS]]: PANDAS is a controversial hypothesis that there exists a subset of children with rapid onset of | * [[PANDAS]]: PANDAS is a controversial hypothesis that there exists a subset of children with rapid onset of OCD or tic disorders and that these symptoms are caused by GABHS infections. The proposed link between infection and these disorders is that an initial autoimmune reaction to a [[GABHS, Group A beta hemolytic streptococcus|GABHS]] infection produces antibodies that interfere with basal ganglia function, causing symptom exacerbations. It has been proposed that this autoimmune response can result in a broad range of neuropsychiatric symptoms. | ||
* Dyskinetic [[cerebral palsy]]: It is a type of cerebral palsy primarily associated with damage to the basal ganglia in the form of lesions that occur during brain development due to bilirubin encephalopathy and hypoxic-ischemic brain injury. Symptoms include slow, uncontrolled movements of the extremities and trunk and small, rapid, random and repetitive, uncontrolled movements known as chorea. Involuntary movements often increase during periods of emotional stress or excitement and disappear when the patient is sleeping or distracted. | * Dyskinetic [[cerebral palsy]]: It is a type of cerebral palsy primarily associated with damage to the basal ganglia in the form of lesions that occur during brain development due to bilirubin encephalopathy and hypoxic-ischemic brain injury. Symptoms include slow, uncontrolled movements of the extremities and trunk and small, rapid, random and repetitive, uncontrolled movements known as chorea. Involuntary movements often increase during periods of emotional stress or excitement and disappear when the patient is sleeping or distracted. | ||
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* Fahr's disease: A rare, genetically dominant | * Fahr's disease: A rare, genetically dominant | ||
* Blepharospasm: It is any abnormal contraction or twitch of the eyelid. Blepharospasm may come from abnormal functioning of the brain's basal ganglia. | * Blepharospasm: It is any abnormal contraction or twitch of the eyelid. Blepharospasm may come from abnormal functioning of the brain's basal ganglia. | ||
=== Entities / Miasms === | === Entities / Miasms === | ||
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* Hypokinetic: Bradykinesia, Rigidity, Tremor, Parkinsonism: [[WEE, Eastern & Western Equine Encephalitis|WEE]] | * Hypokinetic: Bradykinesia, Rigidity, Tremor, Parkinsonism: [[WEE, Eastern & Western Equine Encephalitis|WEE]] | ||
* Hyperkinetic: ChoreAthetosis, Psychosis, Hypertension: [[JE, Japanese encephalitis|JE]] | * Hyperkinetic: ChoreAthetosis, Psychosis, Hypertension: [[JE, Japanese encephalitis|JE]] | ||
=== Notes === | === Notes === |
Latest revision as of 05:22, 8 May 2023
Clinic
- There are three form of basal Ganglia diseases:
- Hyperkinetic disorders: Failing to properly suppress unwanted movements
- Hypokinetic disorders: Failing to properly prime upper motor neuron circuits to initiate motor function.
- Undefined form
Hyperkinetic disorders
- Huntington's disease
- Dystonia: It can occur as a Hyperkinetic or Hypokinetic disorder or as a side effect of disorders such as Parkinson's disease.
- Hemiballismus: It is a hyperkinetic movement disorder that causes uncontrolled movement on one side of the body.
Hypokinetic disorders
- Parkinsonism: Rigidity + Rest tremor + Bradykinesia (Slowness in initiation and execution of movement)
Undefined form
The following diseases that generally involve the basal ganglia do not clearly fit into being either hypo- or hyperkinetic.
- Sydenham's chorea: Characterized by rapid, uncoordinated jerking movements primarily affecting Face / Hands / Feet. It is a result of an autoimmune response that occurs following infection by GABHS that destroys cells in the corpus striatum.
- PANDAS: PANDAS is a controversial hypothesis that there exists a subset of children with rapid onset of OCD or tic disorders and that these symptoms are caused by GABHS infections. The proposed link between infection and these disorders is that an initial autoimmune reaction to a GABHS infection produces antibodies that interfere with basal ganglia function, causing symptom exacerbations. It has been proposed that this autoimmune response can result in a broad range of neuropsychiatric symptoms.
- Dyskinetic cerebral palsy: It is a type of cerebral palsy primarily associated with damage to the basal ganglia in the form of lesions that occur during brain development due to bilirubin encephalopathy and hypoxic-ischemic brain injury. Symptoms include slow, uncontrolled movements of the extremities and trunk and small, rapid, random and repetitive, uncontrolled movements known as chorea. Involuntary movements often increase during periods of emotional stress or excitement and disappear when the patient is sleeping or distracted.
- Athymhormic syndrome: It is a rare psychopathological and neurological syndrome characterized by extreme passivity, apathy, blunted affect, and a profound generalized loss of self-motivation. The syndrome is believed to be due to damage to areas of the basal ganglia or frontal cortex, specifically the striatum and globus pallidus, responsible for motivation and executive functions.
- Lesch–Nyhan syndrome: A rare X-linked recessive disorder
- Wilson's disease: An autosomal recessive genetic disorder
- Fahr's disease: A rare, genetically dominant
- Blepharospasm: It is any abnormal contraction or twitch of the eyelid. Blepharospasm may come from abnormal functioning of the brain's basal ganglia.
Entities / Miasms
- Hypokinetic: Bradykinesia, Rigidity, Tremor, Parkinsonism: WEE
- Hyperkinetic: ChoreAthetosis, Psychosis, Hypertension: JE
Notes
- Hyperkinetic disorders are seen in NMDR encephalitis and also is a kind of Basal Ganglion disorder. So I consider Psychosis, Hypertention and Aphasia for it.
- Hypokinetic disorder, as it said in Athymhormic syndrome, has a Motivation decreasing feature, which is different from Depression. Its quality is similar to Schizophrenia. I think it is catatonic character and not Depressive.