Define the Movement
Movement Disorders
Anatomy
Classic "Signs"
Medications
100

Lack of voluntary coordination of muscle movements

Ataxia

100

MCC of hemiballismus in patient with history of poorly controlled diabetes

Nonketotic hyperglycemia

100

Location of atrophy in Huntington Disease

Caudate

100

Classic MRI sign in Parkinson disease, reflecting loss of the normal nigrosome-1 appearance in the substantia nigra

Absent "swallow-tail" sign

100

5-HT2A receptor inverse agonist in PD psychosis

Pimavanserin

200

Brief, non-rhythmic stereotyped behaviors or utterances associated with a preceding premonitory sensation (involuntary but sometimes suppressible) 

Tics

200

Rare choreiform movement disorder characterized by involuntary, rapid, irregular movements of the limbs, face, and trunk that occurs as a complication of cardiac surgery

Post-pump chorea

200

2 common DBS targets in parkinson disease

1) Globus pallidus internus

2) Subthalamic nucleus

200

 classic sign on MRI of Multiple system atrophy (MSA)

"Hot cross buns" sign

200

Class of medications used in Huntongton's Disesase with black box warning of suicidality secondary to depression

VMAT2-inhibitors 

300

Simultaneous contraction or co-activation of agonist and antagonist muscles, resulting in abnormal stiffness, tremulousness, twisting, or repetitive movements

Dystonia

300

Chorea (arm/leg fleeing with pelvic thrusts), seizures, orofacial dystonia, decreased/absent DTR, abnormal movements lead to gait disturbance; PBS: Acanthocytes

Chorea-acanthocytosis

300

Lesion in Palatal myoclonus

Guillain-mollart triangle

300

 classic sign seen on MRI of Progressive supranuclear palsy (PSP)


“Hummingbird” sign and “morning glory” sign

300

NMDA antagonist used in levodopa-induced dyskinesias

Amantadine

400

sudden, brief, involuntary muscle jerks or twitches; agonist muscle involvement only

Myoclonus

400

nocturnal dyspnea, chorea, and ballismus causing frequent disruption of sleep

- A/w AD nocturnal frontal lobe epilepsy

Paroxysmal hypnogenic dyskinesia

400

Pantothenate kinase-associated neurodegeneration (PKAN) is caused by PANK2 gene mutation on Ch. 20 which leads to iron accumulation here

Globus pallidus

400

what classic sign is seen on MRI of Wilson's Disease

"Panda" sign

400

drug class used in PD that can cause impulse control disorders, sleep attacks, orthostatic HoTN, fibrosis of pleuropulmonary tissue and heart valves 

Dopamine agonists

500

Rapid, high frequency tremor that occurs when standing or weight-bearing that resolves when sitting or lying down

orthostatic tremor

500

Hereditary progressive dystonia with diurnal fluctuations

- GCH1 gene on Ch. 14 (DYT-GCH1)

Segawa disease (Dopa-responsive dystonia)

500

Kufor-rakeb syndrome is caused by neuronal ceroid lipofuscinosis and brain iron accumulation here

deep cortical structures (esp. basal ganglia)

500

 classic sign seen on MRI of Pantothenate kinase-associated neurodegeneration (PKAN)

”Eye the tiger" sign

500

medication to reduce frequency of attacks in episodic ataxia type 2

dalfampridine (4-aminopyridine, K channel blocker)