canine dyskinesia consensus Flashcards

JVIM 2021

1
Q

main output structures of the basal nuclei

A

endopedoncular nucleus, substancia nigria

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2
Q

direct pathway of movement control

A

dopaminergic innervation of caudate/putamen from the substancia nigria increase inhibition of the subsantcia nigria/EPN by activating D1 recept on gabapergic medium spiny neuron. this release the thalamus from tonic inhibition. This increase the excitatory feedback from the thalamus to motor cortex and caudate/putamen.
PROMOTE MOVEMENT

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3
Q

dopaminergic receptor in motor control

A
  • D1 recept: increase glutamatergic activity, direct pathway
  • D2 recept: decrease glutaminergic activity
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4
Q

indirect pathway of movement control

A

medium spiny neurons inhibit GABAergic neuron in globus palidus. This release the subthalamic nucleus from inhibition, increasing excitation of SN/EPN, and in turn inhibition of thalamus. Decrease thalamic excitation of motor cortex and caudate/putamen
INHIBITS MOVEMENT

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5
Q

dopamine promote or inhibit movement ?

A

promote: excite medium spicy neuron through D1 recep in direct pathway, inhibit through D2 in indirect

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6
Q

role of cerebellum in pathophysiology of hyperkinetic disorder

A

lateral cerebellar nucleus conected to striatum via intralaminar nucleus of thalamus

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7
Q

clinical signs resulting from peripheral nerve hyperexcitability

A

fasciculation, myokymia, neuromyotomia, cramps, tentany, tetanus

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8
Q

define myokymia (EMG, channel)

A

continuous contraction of facial/limb myofibers, often exhibiting an **vermicular **movement of the skin overlying the affected muscle.
EMG: burst of single motor unit potential firing at 5-150 Hz
believed to result from abnormal K channel function.
Persist during sleep

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9
Q

define tremors

A

involontary rythmic oscillatory movement of a body part with **symmetric velocity **in both direction of movement.
frequency 1-12 Hz

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10
Q

classification of tremors

A
  1. rest tremors (not in animal)
  2. action tremors: postural (orthostatic, idiopathic head tremors, begnin/idiopathic/rapid postural tremors) and kinetic (intention tremors)
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11
Q

define neuromyotomia (EMG)

A

generalized muscle stiffness with delayed relaxation, often resulting in collapse. Muscle rippling. May be precipited by stress/ excitement
EMG: high frequency (150-300 Hz) burst of decrementing discharge of motor unit potentials with abrubt onset/offset. Spontaneous or initiated by needle movement, volontary contraction percussion of the nerve
Persist during sleep, can be blocked by neuromuscular bloking agent

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12
Q

define cramp

A

sudden, severe, and involuntary muscle contraction or over‐shortening that is generally temporary and benign. Can cause mild‐to‐excruciating pain, and immobility of the affected muscle(s). Onset is usually sudden, and resolves on its own over a period of several seconds, minutes, or hours.
reported with hypoadrenocorticism
EMg: repetitive firing of motor unit action potential at high rate (up to 150 Hz). Number of MU activated and frequency of discharge increase gradually and subside gradually with irregular firing pattern.
Electrically silent cramp with strenous/ischemic exercice in metabolic myopathy associated with defect glycolysis/glycogenolysis

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13
Q

define tetany

A

Sustained muscle contraction, usually involving extensors muscles. No relaxation is noted. May be accompanied by sensory changes (eg, hypocalcemia‐induced tetany).

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14
Q

define tetanus

A

Severe, sustained muscle contraction resulting from impairment of glycine release within the **ventral gray matter **of the spinal cord resulting from exotoxin release associated with Clostridium tetani infections.

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15
Q

epileptic and non epileptic myoclonus

A

Epileptic:
1. Lafora
2. neuronal ceroid lipofuscinosis
3. feline audiogenic reflex seizure
4. juveniel myoclonic epilepsy in Rhodesian Ridgebacks

Non epileptic:
1. Canine distemper virus
2. Startle disease
3. Hemifacial spasm

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16
Q

define myoclonus

A

A sequence of repeated, variably rhythmic, brief shock‐like jerks resulting from the sudden involuntary contraction or relaxation of 1 or more muscles. Generates movement of the affected body part. Differs from a startle response in that myoclonic movements frequently occur independent of a sudden stimulatory input and occur repetitively. May be precipitated or worsened by movement, stress. May occur during sleep.

17
Q

causes of generalised peripheral nerve hyperexcitability

A

hereditary, immune-mediated, paraneoplasic, polyneuropathies, motor neuron diseases, neurodegenerative, metabolic, begnin (stress/exercise), toxicity

18
Q

define athetosis

A

Prolonged slow involuntary contraction of the distal part > trunk muscles resulting in nonrhythmic bending/sinuous/writhing movements. May occur at rest or may be worsened or precipitated by movement.

19
Q

define ballism

A

An **abrupt **involuntary contraction of proximal limb muscles resulting in **large‐amplitude flailing/flinging movements **of the limb(s); typically unilateral.

20
Q

define chorea

A

An abrupt, irregular, and unsustained low‐amplitude contraction of muscle groups, particularly **distal **muscles resulting in 1 or more discrete movements. Similar in distribution to athetosis but faster and larger amplitude. Not characterized by an inserted posture (as in dystonia) but rather an inserted movement.

21
Q

define dystonia

A

A sustained, slow, involuntary contraction of agonist and antagonist muscles of a body region producing abnormal postures and/or involuntary movement of portions of the body along a longitudinal axis. May appear as a twisted posture of the limbs, trunk, or neck. Associated with varying durations of muscle contracture (arrhythmic). Only occurs in wakeful state.

22
Q

define fasciculation

A

A **brief **spontaneous contraction resulting from the spontaneous activation of a small number of muscle fibers, often causing a vermicular movement under the skin.

23
Q

define myoclonic tremor

A

Likely replaced by term rhythmic myoclonus: brief shock‐like myoclonic movements occurring with a **defined unidirectional fast phase **(positive or negative) and a slower recovery phase.

24
Q

define myotomia

A

A disturbance in muscle relaxation after voluntary contraction or percussion. Is most noticeable after a period of rest, and improves with continued activity. Frequently results in noticeable **hypertrophy **of the affected muscles and may lead to diminished joint flexion when walking

25
Q

etiological classification of canine paroxysmal dyskinesia

A

**inherited or presumed inherited: **
* episodic hypertonicity in CKCS
* paroxysmal dyskinesia in Border Terrier
* Scotty cramp
* PD in the soft coated wheaton terrier
* PD inChinooks
* Dancing Dobermann disease
* Paroxysmal kinesigenic dyskinesia in German Shorthaired Pointer
* PD in Labrador and Jack Russel Terrier

Acquired:
* drug administration (propofol, phenobarbital) and structural intracranial lesion
* paroxysmal gluten-sensitive dyskinesia in Border Terrier

25
Q

mutation PD in Kerry Blue terrier / chinese crested

A

SERAC1 (canine multiple sytem degeneration)

26
Q

mutation PD in CKC

A

BCAN

27
Q

mutation PD in Soft-coated wheaten terrier

A

PIGN

28
Q

mutation PD in Shetland Sheepdog

A

PCK2

29
Q

mutation/breed for myotonia congenita

A

miniature Schnauzer, Australian Cattle, Jack Russel Terrier

30
Q

mutation/breed for inherited myokymia

A

KCNJ10
Jack Russel, Parson Russel, Russel terrier, Toy fox terrier, smooth fox terrier, Belgian Malinois, Chihuahua

31
Q

mutation/breed for myoclonic epilepsy (Lafora)

A

EPM2
miniature wire-haired Dashund, beagle

32
Q

muatation/ breed for startle disease (hyperekplexia)

A

SLC6A5
Irish Wolfhound