Neuro Flashcards

1
Q

What are 4 main UMN signs?

A

Increased tone - spasticity, rigidity
Brisk reflexes
Upgoing plantar reflex (Babinski sign)
Reduced power in UMN pattern - upper limb extensors, lower limb flexors

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2
Q

What are 4 main LMN signs?

A

Hypotonia, reduced tone
Reduced power
Wasting and fasciculations
Decreased reflexes

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3
Q

What are definitions for power ratings 0-5?

A

5 - normal
4 - active movement against gravity and resistance
3 - active movement against gravity
2 - active movement with gravity eliminated
1 - flicker of contraction
0 - complete paralysis

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4
Q

Diplegic gait?

A

Signs
* Bilateral problems
* Normal arm swing
* Stiffness both legs
* Flexion at hip, extension of knee and ankle
* Adductor overactivity with scissoring during walking
Ankles - equinovarus

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5
Q

DDx - diplegic gait?

A

Brain
* Prematurity - periventricular leukomalacia
Spinal cord
* Congenital - spina bifida
* Tumour
* Inflammatory
* Traumatic
* Vascular
* Hereditary spastic diplegia

CP

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6
Q

What are definitions for power ratings 0-5?

A

5 - normal
4 - active movement against gravity and resistance
3 - active movement against gravity
2 - active movement with gravity eliminated
1 - flicker of contraction
0 - complete paralysis

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7
Q

Floppy baby - strong/central - features + DDx?

A

Strong floppy - Central
Features
* Decreased axial tone
* Increased peripheral tone
* Hyperreflexia or normal
* Clonus
* Fisting of hands
* Dysmorphic features
* Seizures
* Sleepy, decreased alertness
* Macro-microcephaly
* Global delay (vs isolated motor delay)

DDx
* HIE
* Infection
* Endocrine
* Genetic - PWS, T21, Fragile X
* Structural/cerebral malformations - lissencephaly
* Metabolic (Zellweger)
Neurocutaneous

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8
Q

Floppy baby - peripheral cause - features + DDx?

A
  • Weak
  • Areflexic
  • Tongue fasciculations
  • Ptosis and eye movements
  • Myopathic facies
  • Alert
  • Muscle atrophy
  • Contractures, DDH, ortho
  • FHx neuromuscular

DDx
* Anterior horn - SMA
* Peripheral Neuropathy - infantile neuropathies
* Neuromuscular junction - myaesthenia syndromes
* Muscle - congenital myopathy, congenital muscular dystrophies, congenital myotonic dystrophy, metabolic myopathy

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9
Q

Key Cerebellar Signs?

A
  • D - Dysmetria, dysdiadokinesia, dysarthria, dysphagia
  • A - Ataxic gait, truncal ataxia (titubation)
  • N - Nystagmus
  • I - intention tremor
  • S - Staccato speech,
  • H - Hypotonia - upward pronator drift
    Pendular knee jerk
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10
Q

Signs to differentiate cerebellar vs sensory Ataxia?

A
  • Gait - broad base, staggering in cerebellar, high stepping unsteady in sensory
  • Nystagmus - present in cerebellar, absent in sensory
  • Dysarthria - scanning/staccato speech in cerebellar, absent in sensory
  • Eye movements - normal/slow in cerebellar, sensory sometimes abnormal
  • Romberg - classically neg in cerebellar, pos in sensory
  • Vibration/proprioception - normal in cerebellar, impaired in sensory
  • Finger nose/heel shin ataxia - present in cerebellar, present in sensory
    Reflexes - normal/pendular in cerebellar, absent/present in sensory
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11
Q

DDx for cerebellar lesion?

A

Signs are ipsilateral
* Vascular - haemorrhage, stroke
* Infective - post viral cerebellitis
* Genetic - Fredriech ataxia, ataxia telangiectasia, spinocerebellar ataxia
* Nutritional - Vitamin E
* Toxicity - chemotherapy cytarabine, phenytoin, EtOH
* Tumour - medulloblastoma, metastati
* Metabolic - lysosomal storage disorder
* Demyelinating - GBS, ADEM
Endocrine - Wilson’s

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12
Q

DDx for sensory Ataxia?

A
  • Nutritional - B12 deficiency, B6 toxicity
  • Peripheral sensory neuropathy - Hereditary sensory motor neuropathy
  • Infection - GBS, HIV
  • Toxic - chemotherapy - platin
    Autoimmune - Diabetes, Sjogrens
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13
Q

CN VI Palsy?

A
  • Lateral rectus palsy, can’t abduct eye, horizontal diplopia, esotropia primary gaze
  • Congenital - congenital esotropia, Duane syndrome, Moebius syndrome
  • Any cause of raised ICP
  • Sub-arachnoid space lesions - haemorrhage, infection, inflammation
  • Inflammatory- post viral, demyelinating
  • Pontine glioma
    Otitis media
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14
Q

CN III Palsy?

A
  • Eye down and out, ptosis, fixed dilated pupil
  • Space occupying lesion - suprasellar - craniopharyngioma, pituitary, midbrain
  • Posterior communicating aneurysm
  • Opthalmoplegic migraine
  • Orbital lesion
    Cavernous sinus thrombosis
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15
Q

CN IV Palsy?

A
  • Superior oblique palsy, head tilt away from affected side, vertical diplopia
  • Congenital
  • Raised ICP
  • Trauma
  • Tumour - midbrain
  • Aneurysm
  • Demyelination - ADEM, MS
    Microvascular disease - Diabetes, HTN
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16
Q

Microcephaly DDx?

A

Congenital
· Malformations - lissencephaly
· Chromosomal - trisomies
· Syndromes Angelman, Cri-du chat, FAS, fetal hydantoin
· Hereditary - AR/AD microcephaly, NF1, TS, Sturge Weber

Acquired
· Infection - TORCH, encephalitis, meningitis
· Trauma - perinatal asphyxia, head injury
· Endocrine - hypothyroidism, hypopituitarism
· Metabolic - maternal diabetes, PKU
· Drugs - fetal alcohol, fetal hydantoin syndrome (maternal AEDs)
· Malnutrition

17
Q

Microcephaly Ix?

A

· Path - TORCH screening, karyotype/microarray, newborn screening, TSH, metabolic
· Urine - CMV
· Imaging - skull X-ray.- calcifications, craniosynostosis, CT/MRI - cerebral malformations
CSF - TORCH

18
Q

Cerebellar DDx?

A

VITAMIN
* Vascular - haemorrhage, stroke
* Infective - post viral cerebellitis
* Toxicity - chemotherapy cytarabine, phenytoin, EtOH
* Tumour - medulloblastoma, metastatic
* Acquired - Genetic - Fredriech ataxia, ataxia telangiectasia, spinocerebellar ataxia
* Metabolic - lysosomal storage disorder
* Inflammatory - demyelinating - GBS, ADEM
Nutritional - Vitamin E

19
Q

Key Cerebellar Signs?

A
  • D - Dysmetria, dysdiadokinesia, drift - upward pronator drift
  • A - Ataxic gait, truncal ataxia (titubation)
  • N - Nystagmus
  • I - intention tremor
  • S - Staccato speech, dysarthria
  • H - Hypotonia
    R - reflexes pendular