neurology Flashcards

1
Q

what is a febrile fit?

A

seizure in presence of fever

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2
Q

age of febrile fit

A

6 months to 6 years of age

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3
Q

causes of febrile fit

A

immature brain more susceptible to environmental changes/factors

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4
Q

what increases risk feb fit

A

fam history 1/4 will have one

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5
Q

can be secondary to

febf it

A

uti, urti, gastroenteritis
otitis media
etc

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6
Q

does feb fit increasee risk of epilepsy

A

nuh uh bruh

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7
Q

when does fever occur with feb fit

A

usually precedes convulsions

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8
Q

how long does convulsion tend to last

with feb fit

A

3-6 minutes

tend to occur once in 24 hr

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9
Q

how does convulsion present with feb fit

A
twitching of the face
arms legs
eye rolling
stifness
jerking 
loss of consciousness

generalised tonic clonic

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10
Q

what do you need to rule out when child comes in with query feb fit

A

any serious causes such as meningitis and encephalitis

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11
Q

What can increase seizure risk with febrile fits

A

if > 20 minutes

family hx

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12
Q

what type of seizure is febrile fit

A

temporal lobe

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13
Q

when do you need to do a hospital assessment

with feb fit

A

<18 months
first seizure or was not assessed after first seizure

serious cause
parental anxiety
There is diagnostic uncertainty about the cause of the seizure.
There were any of the following features:
The seizure lasted for more than 15 minutes, or
There were focal features during the seizure, or
recurred in the same febrile illness, or within 24 hours, or
incomplete recovery after one hour.

The child has no serious clinical findings but is currently taking antibiotics or has recently been taking them.

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14
Q

management of feb fit

A
ABCDE 
recovering position
infer over >5-10mins MIDAZOLAM
infection source find
if suspecting mengitis do LP
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15
Q

advice to parents of feb fit

A
reasurrance
protect head
do not restrain or put anything in mouth
remove nearby danger
very common
high temp causes it- no longstanding brain damage
not same as epilepsy and doesn't increase risk -very mariginaly different 
antipyrexical don't help 
1-3 another episode

acute management if happens again-undress. give paracetamol, fluid intake, fan
< 5 mins seek help

When the seizure stops, check their airway and place them in the recovery position.
If the seizure lasts more than 5 minutes give:
Rectal diazepam repeated once after 5 minutes if the seizure has not stopped, or
One dose of buccal midazolam.

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16
Q

doses of rectal diazepam

A

ecommended doses of rectal diazepam (repeated after 5 minutes if necessary) are:
Less than 1 month of age: 1.25–2.5 mg.
1 month–1 year of age: 5 mg.
2–11 years of age: 5–10 mg.

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17
Q

mizadolam doses

A

Midazolam may be given as a single dose by the buccal route (intravenous solution for injection should be administered into the buccal cavity between the gum and cheeks using a syringe or straw), although it is not licensed for this indication. Recommended doses of midazolam are:
Less than 6 months of age: 300 micrograms/kg body weight (maximum 2.5 mg).
6 months–11 months of age: 2.5 mg.
1–4 years of age: 5 mg.
5–9 years of age: 7.5 mg.

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18
Q

when to call ambulance with feb fit

A

all an emergency ambulance if, 10 minutes after the first dose:
The seizure has not stopped.
The child has ongoing twitching (although the larger jerking movements have stopped).
Another seizure has begun before the child regains consciousness.
Measure blood glucose if the child cannot be roused or is convulsing.

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19
Q

nice guidelines about parental advice with feb fit

A

Inform parents about the nature of febrile seizures:
Febrile seizures are not the same as epilepsy. The risk of epilepsy developing later is low but slightly higher than the general population.
Short-lasting seizures are not harmful to the child.
About 1 in 3 children will have another febrile seizure.
Advise parents on what to do if a further seizure occurs. They should:
Protect them from injury during the seizure.
Not restrain them or put anything in their mouth.
Check their airway and place them in the recovery position when the seizure stops. Explain that the child may be sleepy for up to an hour after the seizure.
Seek medical advice if a seizure lasts for less than 5 minutes, or call an ambulance if the seizure continues for more than 5 minutes.
Advise parents about managing fever, but explain that reducing fever does not prevent recurrence. Advice should cover:
When and how to use ibuprofen and paracetamol to reduce fever.
Practical measures on how to reduce fever and prevent dehydration.
When to seek medical help because of prolonged symptoms, or deterioration, especially if there are features of a serious underlying cause for the infection, such as meningitis.
For further information see the CKS topic on Feverish children - management.
Advise parents to continue childhood immunizations even if the febrile seizure followed an immunization.
Do not prescribe drugs to manage or prevent future seizures unless advised to do so by a specialist. This may be advised following assessment of a child with an indication for urgent admission.
Arrange follow-up, the timing of which will depend on the clinical condition of the child.

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20
Q

what is a breath holding attack

how long

A
infant usually or toddler is upset angry or scared they tend to be trigged by trauma or anger
can be caynatoic
appear to stop breathing on exhalation 
its involuntary 
lasts less than. 1min
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21
Q

episodes include

BHA

A

prolonged crying and bread held can lead to cynaosis
grow out by 5 years usually 6 to 18months
F=M

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22
Q

two types of BHA

A

cyanotic and pallid spells

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23
Q

describe each bHA

A
cyanotic
preceipated by crying 
 very upset
deep breath
cyanotic
limb extend 
may be stiff or floppy
cn become unconscious for less than a min
involuntary
not dangerous
breathing resumes after a gasp
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24
Q

what Does it increase risk of later on with BHA

A

vasovagal attacks

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25
Q

what about pallid spells

A

a reflex anoxic seizure
6months -2years
no epielspetic

mostly due to shock or pain or sudden fright
triggers including minor injury and bump on head
more of a vagal reflex
overactivity transient bradycardia and circulatory imapriement
may or may not cry
turn pale and collapse
stiff>floppy
less Lilkely to cry
gasp as they come around
traient apnoea and limpness may look grey

grow out of
place in recovery position

pale limp unconscious –> tonic clonic phase
30-60seconds

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26
Q

management of breath holding attacks

A
eeg
reassurance to parents
stay calm
lie child on side
wartch
avoid shaking 
don't put anything in mouth
don't splash with water
rest child
don't punish or reward
see gp and have leg after first episode esp if under 6 months or if frequent, confusion of lasting more than a min
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27
Q

important thing to rule out with BHA

A

iron deficiency

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28
Q

how many cases of epilepsy in uk

A

600,000

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29
Q

what is epilepsy

A

inappropriate signalling sensory and monitor activity is abnormal - causing activity to be disorder
can be caused be infection fever syncope space occupying lesions

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30
Q

in lay man terms epilepsy

A

signals travel from brain to all parts of body in order to carry out activities and function
in epilepsy these signals are jumbled
causes repeated bursts of electrical activity in the brain

symptoms include:uncontrollable jerking and shaking – called a “fit”
losing awareness and staring blankly into space
becoming stiff
strange sensations – such as a “rising” feeling in the tummy, unusual smells or tastes, and a tingling feeling in your arms or legs
collapsing

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31
Q

two categories of epilepsy

A

focal: locales part of brain (frontal, temporal)< usually no loss of consciousness
generalised: both hemisphere involved - atonic, tonic, myoclonic, etc

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32
Q

management acute setting
three crucial things.
0-5 mins

A

0-5 mins, ABCDE

check glucose IV access

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33
Q

what if it lasts >5 mins seizure

A

5-15mins
same bt also LORAZEPAM
or midazlam If no iV access

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34
Q

what if it lasts >25 mins seizure

A

phenytoin or phenarbital

if not iv access paraldehyde

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35
Q

and over 45 mins seizur

A

PICU and consider putting to alesp with thiopental whilst ventilated and wean slowly
RARE

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36
Q

things to cover in history

seizure

A
what happened before during and after
witness
EEG done before
video telemetry MRI
advice- do not lock bathroom door at home, shower > bath 
helmet when cycling
tell lifeguard when sweimming
driving-need to be fit free
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37
Q

sepsis mx

A

LP
BUFALO
general cephalosporins
Xray

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38
Q

what is infantile spasm

A
-repeated flexion of trunk
forceful and throws arm up
less steady on feet
can draw or use cutlery 
half outgrow, half have pathology 
may have future seizure or DD
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39
Q

what would EEG show for infantile spasms

A

synchronous spikes

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40
Q

west syndrome

A
350-400 in uk
severe epilepsy syndrome 
triad of:
1. infantile spasms 
2. hypsarrthmia 
mental retardaation

eeg patterns

within first year
attacks-> brief and infrequent

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41
Q

treatment of infantile spasms and west syndrome

A

IS; vigabrain, steroid, acth (3)

WS: VIAGBARITIN , COTISOCETIODS, MITRAZPAM, NA VALPORATE (4)

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42
Q

what is spina bifida?

A

neural tube defect

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43
Q

how does it occur spina bifid a

A

failure of neural tube to close in pregnancy

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44
Q

symptoms of spina bifida

A

lemon shaped skull (Arnold chiari malformation)
tuft of hair on lower back
weakness or total paralysis of the legs
bowel incontinence and urinary incontinence
loss of skin sensation in the legs and around the bottom – the child is unable to feel hot or cold, which can lead to accidental injury
Many babies will have or develop hydrocephalus (a build-up of fluid on the brain), which can further damage the brain.
Most people with spina bifida have normal intelligence, but some have learning difficulties.

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45
Q

risk factor for spina bifida

A

folic acid deficiency in pregnancy

fhx

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46
Q

diagnosis

A

tected during the mid-pregnancy anomaly scan, which is offered to all pregnant women between 18 and 21 weeks of pregnancy.

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47
Q

treatment of spina bifida

A

surgery soon after birth to close the opening in the spine and treat hydrocephalus
therapies to help make day-to-day life easier and improve independence, such as physiotherapy and occupational therapy
assistive devices and mobility equipment, such as a wheelchair, or walking aids
treatments for bowel and urinary problems

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48
Q

what is muscular dystrophy

A

x linked autoressive condition causing abnormality to dystrophin protein

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49
Q

how does it present muscular dystrophy

A

motor milestone delay and sometimes mild speech delay

progressive condition

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50
Q

signs and symptoms muscle dystrophy

A
waddling lordotic gait 
calf hypertrophy 
sparing of facial and bulbar muscles 
muscle spasm
respiration difficulty
poor  balance
muscle wasting
sclerosis 
inability to walk
weakness to limb girdle
weakness to limbs or paralysis
51
Q

name a sign and what it is with muscular dystrophy

A

gowen sign

weakness to limb girdles

52
Q

diagnosis of muscular dystrophy

A

creatinine kinease
biopsy
fhx

53
Q

management of muscular dystrophy

A

supportive as no cure
walking aids
scolosis surgery
physiotherapy

54
Q

what are the subtypes of muscular dystrophy

A

becker same as below but later in life
Duchenne-most common, boys, childhood
faciospaculohumeral
myotonic -2nd most common any age

55
Q

what are tics

management

A

repetition of an action of phrase
which causes interferences in daily life
managed by guanfacine

56
Q

what is phlagiocephaly

A

soft skull causing flattening of head on one side

making it look asymmetrical

57
Q

what else can be apparent? with pahgiocqephaly

A

misaligned ears

58
Q

how to prevent phlgioephaly

A

tummy Time
don’t keep in same position for too long
hold both sides

59
Q

risk factors for phaigiocelpahy

A

prematurity
lack of amniotic fluid in prgnancy
also, sleeping on back

60
Q

what is hydrocephalus

A

increase in CSF volume causing dilatation of ventricles

and increases pressure in skull

61
Q

two classifications of hydrocephalus

A

communicating and non comm

62
Q

difference between two types

A

non comm-obstruction in ventricular system

whereas comm-reabsorption failure of CSF

63
Q

examples of comm

A

subarachnoid haemorrhage

menigitis

64
Q

non comm example

A
congenital
atresia
vascular malformation
toxoplasmosis
Arnold chiari malformation -lemons shaped skull
65
Q

presentation of hydrocephalus

A
headache
nausea and vomiting
blurred vision
sunsetting eyes
papillodema
bulging frontalle
dysfunction at sutures 
dilated scalp veins 
rapid increase in head circumference
can be seen with mumps, rubell and spina bifida
later on - six nerve palsy and unstrady gait
66
Q

investigations of hydrocephalus

A

ct mri

67
Q

management of hydrophcephalus

A

shunt

or endoscopic 3rd ventriculostomy

68
Q

what is sunsetting sign

A

white slecera above iris
ocular globes deviated downwards
upper lids retracted

69
Q

later symptoms of hydrocephalus

A

high pitched cry
siezures
train of resp depression, hypotension and bradycardia

70
Q

what is macwens sign

A

cracked pot sound on percussing head

71
Q

give a list of types of headaches

A
raised ICP
infection e.g. mengitisis
analgesic 
hypertension
dental caries
sinusitis
migraine
eye strain
tension headache
72
Q

questions in hx to ask with headache

A

location
fhx e.g. migraine
OCP

73
Q

which type can aura, halo and. zigzag lines be seen in

A

migraine

also throbbing

74
Q

worse in morning or when lying down

A

raised ICP

75
Q

what are focal neurological signs with headache

A
ataxia
nystagmus 
tremor
cranial nerve palsie
seizures
psasticity
endrocrine dysfunction
76
Q

describe tension headache and mx

A

tight bans across front
at end of day
normal exam
reassurance and analgesia

77
Q

migraine with aura

A
throbbing
unilateral
last a few hours
triggers-cheese, caffeine, OCP, Alcohol, chocolate, sleep deprivation, orgasms etc 
aura!!!! 
nausea

rest and nalagesia
pizotifen and proponalol as prophylatic

78
Q

without aura

A

bilateral pulsatatile
photophobia
worse with eercise
same management as above

79
Q

cluster heada he

A
sudden onset
unilateral
perobrial pain 
attacks in clusters
a few times a day
red eye
swelling around eye or tears
rihoarrhea etc 
SUMPITRIPTAN  CCCB - nIFEPIDINE
80
Q

RAISEd icp

A
papillodema 
ataxia
ofocial signs
hypertension
bradycardia
n+v 
vomiting
worse when lying down and localised to sign
CT/.MRI
treat cause
81
Q

migraine is caused by

A

brainstem changes
as it interactions with trigmeinal nerve
imbalance in brain chemicals which regulars pain
also serotonin drop

82
Q

red flags in a migraine history

A
  • short history or recent recurrent severe headache
    change in chracater
    symptoms indicating ICP riaised
    changes in vision and personality
    history of malgnonancy, neurocutenaous syndromes
    young age < 3y/o
83
Q

what is most common headache type in kids

A

migraine

mostly genetic predisposition

84
Q

investigations with headache

A

head circumference and fundoscopy

may only need future if hx od headtrauma or seizure or significant symptoms indicating for ct/mri

85
Q

management with headache migraines

A

reasaurrance
paracetamol and nsaids
antienemtics- metoclopramide, prochlorperazine
then sumatriptan

prolphyatic - proponanol, piztifen na valoproate or topiramate

86
Q

side effects of beta blockers and piztotifen

A

pizotifen -weight gain and sleepiness

bb- contraindicated in asthma

87
Q

head injuries when do you admit

A
if unconsciousness
no parent around
suspected NAI
persisting headache or vomiting
evidence of skull fracture
88
Q

difference between subdural and epidural injury

A

subdural -cresent shape

epidural - lenticular shape

89
Q

causes of subdural haemorrhage

A

2ndary tp jead trauma
elderly
anticoagulation high fall risk patients e.g. e[ileptics

90
Q

pathologyy presentation ix and rx

A
- tearing of veins between sinuses and may cause increase ICP and coning
insidious onset
consciousnesses fluctuating
headache
personality changes and unsteadiness
ct head 
surgical - burr hole
91
Q

extradural haemorrhage

A
2ndary to traume
fractured temporal and parietal bone following trauma to temple just lateral top eye
laceration of middle meningeal vessels and blood accumulation between bone and dural
lucid interval of cosuonessess
headache and vomiting
bradycardiaa and hypertension 
altered mental state 
drop In consciousness as icp increases
hyper-reflexia
xr skull and ct head
lp  is contridincdicated
ligation of bleed
92
Q

management

A

ct within an hour and radiology report withn an hour
indications : nai
post traumatic seizure -1s ttime
GCS < 14
ONE OR DEPRESSED SKULL FRA CTURE
FOCIAL NUEROLOGICAL DEFICITES
AGED <1 WITH BURISE SWELLING OR LACERATION > 5CM ON HEAD

93
Q

ALSO CAN BE IF MORE THAN 1 OF THE FOLLOWING IS PRESENT

A
abnormal drowsiness 
3 or more discrete vomiting eispidoes 
dangerous mechanism -sta, fall from > 3m 
 anmnesia
witnessed loss of consciousness > 5mins

if only one present
observe for four hours and if any other develop then do ct scan

94
Q

seizure with face cheek twitching

A
centrotemporal spikes (BCECTS
 most common epilepsy syndrome in childhood. 

outgrow the syndrome (starts) of 3–13 - a peak around 8–9 years

one side of face or upper limb

95
Q

BHA things to tell parents

A

not harmful
no long term risks

I appreciate its hard to watch as a parent, but key is to stay calm and offer reassurance to child when out of episode

96
Q

which BHA is most common

A

cyanotic 85%

97
Q

what med been found to help BHA

A

Piracetam

even iron in absence of iDA

98
Q

triggers for seizure

A
  • Watching television (although watching with one eye covered presents seizures)
  • Lack of sleep
  • Flashing lights
  • Loud noises
99
Q

tonic and clonic seizure

A

o Tonic – with sustained contraction and stiffness (from ‘tone’)

o Clonic – with rhythmic jerking of one limb, one side, OR the whole body

100
Q

symptoms if occipital affects

A

bright light vision changes

101
Q

pareital

A

sensorimotor

102
Q

Status epilepticus

A
  • Technically, StE is a seizure lasting for >30 min OR repeated seizures lasting >30 min without recovery of consciousness in between
103
Q

post iticialwhat is it and sx

A

After = post-ictal

  • Headache
  • Confusion
  • Myalgia
  • Temporary weakness – after focal seizure in motor cortex (Todd’s palsy)
  • Dysphasia – after focal seizure in temporal lobe
  • Sore tongue (bitten during seizure)
104
Q

what do u need to exclude with west syndrome and what is first line mx

A

prednisolone

tuberous sclerosis

105
Q

most common in children type of epilepsy

A

⮚ rolandic benign
Predominantly nocturnal sensorimotor seizures
⮚ Onset in one side of face/ a hand, then spreading down one side and may generalise

106
Q

mx difference focal/partial and generalised

A

partial - carbamazepine and sodium val

generalised -sodium val and lamtrogiene

107
Q

meds for hydrocephalus

A
  • Furosemide and acetazolamide → inhibit CSF secretion by choroid plexus
  • Isosorbide → promotes resorption
108
Q

diagnostic criteria migratne w/o aura

A

A. At least 5 attacks fulfilling B-D
B. Headache attack lasting 1-48h
C. Headache has at least 2 of the following:
a. Bilateral (temporal or frontal) OR unilateral location
b. Pulsating quality
c. Moderate-to-severe intensity
d. Aggravation by routine physical activity
D. During headache, at least 1 of the following:
a. Nausea and/or vomiting
b. Photophobia and/or phonophobia

109
Q

migraine with aura

A

Idiopathic recurring disorder: headache that usually lasts 1-48h
B. At least 2 attacks fulfilling C
C. At least 3 of the following:
a. 1/more fully reversible aura symptoms indicating focal cortical and/or brainstem and and and dysfunction
b. At least 1 aura developing gradually over >4 min, or 2/more symptoms occurring in and and succession
c. No aura lasting >60min
d. Headache follows in <60min

110
Q

pathological cause of plagiocepahly

A

the plates of the skull fusing together too early = craniosynostosis

111
Q

diagnostic criteria four things for tics

A
  1. Multiple motor tics AND one/more vocal tics starting <18 years
  2. Presence for >1 year (may occur many times a day or be intermittent)
  3. significant functional impairment
  4. NOT due to drug abuse or secondary causes
112
Q
  • Echolalia
A

copying others words

113
Q
  • Palilalia =
A

repeating own words

114
Q

coprolalia

A

foul words inappropriate repeated

115
Q

copropraxia

A

obscene gesturees

116
Q

echopraxia

A

copying others movements involuntary

117
Q

tics severity rating

A

MOVES scares

118
Q

how many are symptom free by adults with tics

A

1/3

119
Q

meds for tics

A
first choice
licensed 
halipdersol
can also
use risperdone
120
Q

myotnic dystrophic risk with surgery

A

malignant hypertehermia risk increases

121
Q

myotonic dystrophy

A

tent shaped mouth

122
Q

spina bifidis back presentations

A

no herniation of numeral tissue with spina bifida occult
spinal USS or MRI

Meningocele:

  • Herniation of meninges and fluid only with skin covering
  • Rx: requires surgical closure
  • Prognosis: excellent prognosis :)

Myelomeningocele:
- Herniation of spinal neural tissue, which may be covered by meninges/skin OR be open

123
Q

problem with myelomeningiccele

A
o	Flaccid paralysis below the lesion
o	Urinary and faecal incontinence
o	Urinary tract dilatation
o	Hydrocephalus
o	Bulbar paresis secondary to Chiari malformation
o	Vertebral anomalies (e.g. kyphosis)