Neuro and development Flashcards

1
Q

Paediatric autoimmune neuropsychiatric disorders associated with strep infections (PANDAS)

A

Child with Tourettes, tics, OCD, anorexia plus infection.

ABx plus risperidone.

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2
Q

3 core areas affected in ADHD

A

Inattention
Hyperactivity
Impulsivity

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3
Q

ADHD definition

A

Attention deficit and hyperactivity disorder.
Persistent behaviours (longer than 6months) and inferring with social, academic or occupational performance.
Start before 12yrs.
Occurs in 2 or more environments.

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4
Q

Manifestations of Inattention

A

Disorganised
Difficulty following instructions
Disorganised and loosing items.
Easily distracted

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5
Q

Manifestations of hyperactivity

A

Fidgeting
Tapping
Talkative
Climbs over things

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6
Q

Manifestations of impulsivity

A

Poor road safety
Interrupting speech
Answers before complete questions asked.
Unable to take turns or share.

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7
Q

Some environmental factors in the aetiology of ADHD

A
Maternal smoking or alcohol consumption during pregnancy.
Parental co-morbidity.
Low birth weight.
Preterm delivery.
Psychosocial adversity.
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8
Q

Common ADHD patient

A

MALE

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9
Q

Differentials for ADHD patients

A

Autism spectrum disorder.
Personality disorder.
Fetal alcohol syndrome.
Auditory or visual impairment.

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10
Q

Investigations and diagnosis of ADHD

A
Behavioural observation (NB symptoms are not constant)
Discuss with teachers
CLINICAL DIAGNOSIS
Conner's scale
Screen for organic cause.
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11
Q

Treatment of ADHD

A
Non-pharm =  patient CBT, positive parenting.
Pharm = Ritalin/Methylphenidate 1st line, Atomoxetine 2nd line
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12
Q

Definition of Autism Spectrum Disorder

A

Persistent disorder, present from childhood which causes significant impairments to ADLS of patient. There are significant deficits in social communication, social interaction and restricted repetitive behaviour/interests patterns.

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13
Q

Common autism spectrum disorder patient

A

MALE. Present when patient’s capacity is not enough to manage social demands, despite it being present since childhood.

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14
Q

Risk factors for ASD

A

Preterm (before 35weeks)
Sibling with ASD
FHx of mental health problems e.g. schizophrenia.
Maternal sodium valproate in pregnancy.
Congenital conditions such as cerebral palsy, Downs, neonatal encephalopathy.

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15
Q

Manifestations of impaired social communication in ASD

A
Lack of close friendships.
Enjoys privacy.
No appreciation for others/lack of empathy.
Lack of acting to social cues
Avoid gaze
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16
Q

Manifestations of restricted, repetitive behaviours

A
Stereotype movement (spinning).
Narrow fixations.
Insists on following routine.
Distress/tantrum over change.
Echolalia
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17
Q

Other manifestations of ASD

A

Impaired imagination = abnormal communication.

Language delay/regression.

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18
Q

Investigating ASD

A

Specialist team.
Collateral info from school.
Observe behaviour in different settings.
Diagnostic instruments e.g. Autism Diagnostic Observation Schedule or diagnostic interviews.

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19
Q

Management of ASD

A

Early intensive behavioural intervention e.g. applied behavioural analysis.
Speech therapy.
Parental training and education.

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20
Q

Risk factors for cerebral palsy

A
Preterm
Low birth weight
Neonatal encephalopathy
Neonatal sepsis
Neonatal meningitis
Chorioamnionitis
21
Q

Some causes of cerebral palsy

A
Antenatal = TORCHS infections = vascular occlusion, structural maldevelopment.
Postnatal = Hypoxic-ischaemia injury, intraventricular haemorrhage, hyperbilirubinaemia. 
Preterm = periventricular leukomalacia.
22
Q

Definition of cerebral palsy

A

Umbrella term used to describe permanent motor dysfunction resulting in postural and movement abnormalities. Caused by non-progressive lesion in developing brain.

23
Q

Symptom progression in cerebral palsy

A

Lesion to brain is non-progressive, however, as brain and cerebrum develops with aging manifestations of the lesion change.

24
Q

Some clinical features of cerebral palsy

A
Paucity in movements
Hypotonia, spasticity, dyskinesia.
Poor head control, rolling or crawling.
Persistent primitive reflexes.
Feeding difficulties.
Not sitting by 8months
Not walking by 18months.
Asymmetry in hand function before 12months.
25
Subtypes of cerebral palsy
Spastic - further divided in hemiplegia, diplegia, quadriplegia. Dyskinetic - involuntary movements. Ataxic Mixed
26
Differences between subtypes of spastic cerebral palsy
``` Hemiplegia = unilateral arm and leg involvement with arm > leg. Diplegia = legs > arms. Quadriplegia = all 4 limbs and trunk with seizures. ```
27
Management of cerebral palsy
MDT = community paediatrician, SALT, nurse, dietician, physio, OT, social worker. Analgesia if in pain. Botulinum toxin for excessive, painful spasticity.. Manage co-morbidities.
28
Differentials for delay in walking
Duchenne muscular dystrophy. Birth trauma/DDH. Spina bifida. Global developmental delay
29
Causes of global developmental delay
``` Down syndrome Fragile X Duchenne muscular dystrophy Hydrocephalus Prenatal alcohol or smoking. Congenital infections (TORCHS) Periventricular leukomalacia. Hyperbilirubinaemia Hypoglycaemia Meningitis and head injuries. ```
30
Primitive reflexes
``` Palmar reflex Plantar reflex Rooting reflex Moro reflex Asymmetrical tonic neck reflex. ```
31
Significance of persistent primitive reflexes
Neurodevelopmental pathology eg Cerebral palsy
32
Significance of asymmetrical primitive reflex
Peripheral neuropathy or CNS lesion
33
Onset and disappearance of primitive reflex
Onset = 28wks gestation. | Go by as postural reflexes appear. 6months?! CHECK
34
Features of a tonic clonic seizure
Stiff limbs, jerking, LOC
35
Absence seizure
Brief period of unawareness/vacany and staring, eyes may roll back Rx = valproate
36
West syndrome
Infantile spasm - 5months Head nodding, arm jerks EEG = hypsarrythmia Rx = prednisolone then vigabatrin
37
Myoclonic jerks/juvenile myoclonus
1-4yrs, mor common in femaless Most after waking up. Throwing items which are in patients hand. Ix = EEG polyspike, photosensitive pattern. Rx = sodium valproate 1st line, Keppra 2nd line 2/3 at risk fo GTC in later life.
38
Causes of seizures in children
``` CNS tumour Idiopathic Cerebral vascular occlusion Febrile seizure Hypoglycaemia Hypocalcaemia/magnesaemia/natraemia. Meningitis or encephalitis. ```
39
Clinical features of a febrile convulsion
Generalised tonic clonic, symmetrical seizure. Fever/pyrexia. Rx = recovery position, if lasting >5mins buccal midazolam/IV lorazepam. Parent reassurance and education. If simple no risk of developing epilepsy, complex do have increased risk.
40
Reflex anoxic seizure
Vagal inhibition = cardiac asystole = syncope. Provoked by pain and discomfort. Pale, atonic (falls to floor), tonic-clonic movements. EEG = slow wave discharge.
41
What to monitor with patients on Ritalin
weight and height
42
Definition of failure to thrive
Failure to gain adequate weight or grow at normal rate for ages. Suboptimal weight gain. Need 2 measurements 3-6months apart showing child fall across 2 major centiles.
43
Panayiotopoulos syndrome
Seizure of autonomic symptoms occurring mainly at night and can last over 30mins. Pale, vomiting, pupil dilation, sweating.
44
Differentials for a seizure
Benign myoclonus of infancy Arrhythmia Daydreaming - ASD Syncope
45
Organic causes of a seizure
``` Infection Hypoglycaemia Hyponatraemia Low calcium or magnesium Chemotherapy Lack of sleep ```
46
Causes of hydrocephalus
Infection/meningitis = non obstructive. Subarachnoid haemorrhage Aqueduct stenosis Chiari malformation
47
Features in hydrocephalus
Large head Bulging fontanelle Downward gaze = sunsetting eyes Raised ICP = headache, papilledema, n+v
48
Ventricles in hydrocephalus
dilate superior to obstruction in CSF flow
49
Treatment for hydrocephalus
LP | Ventriculoperitoneal shunt