Category
page 1Extrapyramidal and movement disorders
Huntington's disease
rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia
restless legs syndrome
disabling neurological pathology characterized by the irresistible urge to move the legs
choreatic disease
Chorea, or (rarely) choreia, () is an abnormal involuntary movement disorder, characterized by quick movements of the hands or feet. It is one of a group of neurological disorders called dyskinesias. The term chorea is derived , as the movements of the body are comparable to dancing.
stiff-person syndrome
rare neurologic disorder characterized by progressive rigidity and stiffness in truncal muscles, spasms, postural deformities, chronic pain, impaired mobility, and lumbar hyperlordosis
dystonia
Dystonia is a neurological hyperkinetic movement disorder in which sustained or repetitive muscle contractions occur involuntarily, resulting in twisting and repetitive movements or abnormal fixed postures. The movements may resemble a tremor. Dystonia is often intensified or exacerbated by physical activity, and symptoms may progress into adjacent muscles.
blepharospasm
Blepharospasm is a neurological disorder characterized by intermittent, involuntary spasms and contractions of the orbicularis oculi (eyelid) muscles around both eyes. These result in abnormal twitching or blinking, and in the extreme, sustained eyelid closure resulting in functional blindness.
progressive supranuclear palsy
neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia
neuroleptic malignant syndrome
nervous system disease that is characterized by hyperthermia, muscular rigidity, autonomic dysfunction and altered consciousness and is associated with administration of antipsychotic and other central dopaminergic blockers
multiple system atrophy
neurodegenerative disorder characterized by autonomic failure, parkinsonism, cerebellar impairment and corticospinal signs, with a median survival of 6-9 years
essential tremor
movement disorder causing involuntary tremors, especially in the hand
myoclonus
Myoclonus is a brief, involuntary, irregular (lacking rhythm) twitching of a muscle, a joint, or a group of muscles, different from clonus, which is rhythmic or regular. Myoclonus (myo- "muscle", clonus "spasm") describes a medical sign and, generally, is not a diagnosis of a disease. It belongs to the hyperkinetic movement disorders, among tremor and chorea for example. These myoclonic twitches, jerks, or seizures are usually caused by sudden muscle contractions (positive myoclonus) or brief lapses of contraction (negative myoclonus). The most common circumstance under which they occur is whi
parkinsonian syndrome
Parkinsonism is a clinical syndrome characterized by tremor, bradykinesia (slowed movements), rigidity, and postural instability.
dyskinesia
Dyskinesia is a category of movement disorders that are characterized by involuntary muscle movements, including movements similar to tics or chorea and diminished voluntary movements. Dyskinesia can be anything from a slight tremor of the hands to an uncontrollable movement of the upper body or lower extremities. Discoordination can also occur internally especially with the respiratory muscles and it often goes unrecognized. Dyskinesia is a symptom of several medical disorders that are distinguished by their underlying causes.
extrapyramidal symptoms
drug-induced movement disorders
movement disorders
clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements
pantothenate kinase-associated neurodegeneration
neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13
cervical dystonia
human disease
hemiballismus
Hemiballismus or hemiballism is a basal ganglia syndrome resulting from damage to the subthalamic nucleus in the basal ganglia. It is a rare hyperkinetic movement disorder, that is characterized by pronounced involuntary limb movements on one side of the body and can cause significant disability. Rarely it affects both sides of the body. Symptoms can decrease during sleep.
hemifacial spasm
neurologic disorder
Meige syndrome
cranio-facial dystonia that is accompanied by blepharospasm
intention tremor
dyskinetic disorder characterized by a broad, coarse, and low frequency tremor
Rabbit syndrome
drug side effect

ioflupane I-123
chemical compound
myoclonic dystonia
dystonia characterized by myoclonic jerks affecting mostly proximal muscles and dystonia, usually torticollis or writer's cramp, that typically responds to alcohol and has onset in the first of second decade of life
neurodegeneration with brain iron accumulation
neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia
postencephalitic Parkinson disease
disease believed to be caused by a viral illness that triggers degeneration of the nerve cells in the substantia nigra. Overall, this degeneration leads to clinical parkinsonism
deafness dystonia syndrome
mitochondrial metabolism disease that is characterized by hearing loss that begins early in life, problems with movement, impaired vision, and behavior problems
Lance–Adams syndrome
sequela of hypoxic encephalopathy
chorea gravidarum
Human disease
motor disorder
neurodevelopmental motor disorder
mirror movement disorder
movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs