Paediatric Neurology Flashcards

1
Q

name other words for disorder.

A

Disability

Syndrome

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2
Q

Give a few examples of syndromes seen in children.

A

22 deletion syndrome
Fragile X syndrome
Epilepsy
Fetal Alchohol syndrome

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3
Q

How are developmental disorders identified?

A
  • Neonatal Health Screening
  • Health visitor visits and reviews
  • Orthoptist vision screening
  • follow up if “high risk” infants
  • listening to parents
  • opportunistic recognition
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4
Q

When is the onset of a neurological disability?

A
It can be:
Pre-Natal
Peri-Natal
Post-Natal
Evolving process over first few weeks or months of life
Sudden event (traumatic/non-traumatic)
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5
Q

Who are key participants in the rehabilitation process?

A

Parents

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6
Q

What are some signs between birth and 3 months that would flag something isn’t quite right?

A
  • difficulties with muscle tone (floppy/rigid)
  • large/small head
  • jerking of limbs
  • inability to feed (poor suck/ coordination)
  • excessive irritability
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7
Q

From 3 months to 3 years what problems can appear?

A
  • developmental delay
  • progressive disorder
  • visual difficulties
  • disorders of language, communication and mechanics of eating
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8
Q

Name this:
Generalised motor and/or cognitive delay
gross/fine motor delay
symmetrical/asymetrical

A

Developmental Delay.

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9
Q

Name this:

The loss of skills or inability to gain skills.

A

progressive disorders

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10
Q

For disorders of language, communication and mechanics of eating, what should we look out for?

A
  • Can’t gain weight
  • Speech delay or DLD
  • Hearing/ENT disorder
  • Autistic Spectrum Disorder (ASD)
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11
Q

name a visual difficulty.

A

delayed visual maturity

or could be blind

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12
Q

What disorders tend to appear from 3-16 years?

A
  • Seizure Disorders
  • Neuromuscular Disorders
  • Brain Injury- non traumatic or traumatic
  • Degenerative conditions
  • Neurobehavioural Disorders
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13
Q

At what age range do: headaches and neurological sleep disorders, appear?

A

5 to 16 years.

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14
Q

How may a child be referred?

A
  • GP
  • Parental Awareness
  • Nursery/school
  • A and E department
  • Health Visitor
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15
Q

What is the focus of child development services?

A

It is centered around the child (and their family) .

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16
Q

How are children assessed?

A
  • collation of information from primary care and referrers
  • home visit
  • paediatrician assessment
  • allied health professional assessment
  • liason with education services
17
Q

What is essential between professional teams?

A

communication

Information sharing.

18
Q

What is required in assessment?

A
  • Background History
  • Parent/Carer perspective
  • Child’s perspective
  • Developmental Assessment
  • Physical Examination-Diagnostic formulation and targeted investigations
  • monitor developmental process over time
  • assessment by other specialists e.g. genetics
19
Q

Why should we look for an aetiology?

A
  1. to inform functional impact and prognosis
  2. to allow accurate counselling for parents
  3. allows appropriate support and early intervention
  4. stops further intrusive and possible painful investigations.
20
Q

What kind of investigations are done?

A
  • Invasive/ Non-Invasive
  • Neurological examination
  • Video analysis
  • Diaries
  • EEG, MRI scan etc.
21
Q

Name the components of the ICF WHO.

A

Health Condition (disorder/disease)

Body functions and structure, Activity & Participation

Environmental and Personal factors (aka contextual factors)

22
Q

What are some common problems in children with complex disabilities?

A
  • saliva control difficulties
  • feeding problems
  • gastro-oesophageal reflux
  • mobility problems
  • communication difficulties
  • pain
23
Q

What are some other issues to consider apart from the childs’ disorder?

A
  • Family Perspective
  • Process of adjustment
  • Traumatic event
  • Bereavment Process.
24
Q

Generally, how can having a child with a disability impact the family?

A
  • Increased stress
  • loss of relationships/friendships
  • poor parental health
  • high level of stress when dealing with service providers.
25
Q

What are some problems when a parent comes to and SLT with their disabled child?

A
  • They don’t understand where we fit in/ what our role is.
  • lack of understanding of mechanics of speech
  • parent expectations different from treatment plan
26
Q

It is important to view parents as ______ and form a _______ ________.

A

Equals

working relationship.

27
Q

The diagnosis of neuro-disability in a child has a devastating impact on the ______, their ______, ______ and _______ _________.

A

Child
Parents
Siblings
Extended Family

28
Q

Diagnosis triggers _______ _______.

A

powerful emotions.

29
Q

What can vary when it comes to diagnosis?

A

Parental Reactions to the diagnosis. (good/v. bad)

30
Q

What’s essential to support clinical diagnosis and treatment plans?

A

knowledge of child development.

31
Q

Good _____ must be established between the SLT and parent.

A

communication.

32
Q

What is rated highly in parental expectations?

A

The importance of pleasurable feeding experiences for children.

33
Q

Why is communication between all members of the professional team essential?

A

In order to have a wider undertsanding of the child’s clinical needs (and family dynamics). Allows you to provide a more hollistic approach to care.