Medically Compromised Child Part 2 Flashcards

(30 cards)

1
Q

How many weeks is pregnancy

A

41 weeks

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2
Q

what does the 11-14 week scan show

A

to confirm viability of pregnancy
to confirm how many there are
to outline expected delivery date
optional blood tests offered to screen for:
Down syndrome
Edward syndrome
pat syndrome

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3
Q

what is the most common chromosomal abnormality

A

Down Syndrome

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4
Q

when is the major abnormality scan

A

20 weeks

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5
Q

what is picked up on the 20 week scan

A

spina bifida
cleft lip and palate
anomaly scan

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6
Q

what can whooping cough and RSV vaccines cause

A

serious illness and breathing difficulties

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7
Q

who and when should have whooping cough and RSV vaccines

A

pregnant mothers

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8
Q

what is respiratory syncytial associated with

A

bronchiolitis and pneumonia in young babies

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9
Q

what is strep B in pregnancy associated with

A

late miscarriage and stillbirth

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10
Q

possible causes of meningitis

A

viral
bacteria
TB
Group B strep
E coli

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11
Q

what can meningitis cause

A

brain injury
hearing and sight loss
behavioural changes
amputation
enamel defects

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12
Q

what does the heel prick test assess for

A

sickle cells
cystic fibrosis
congenital hypothyroidism
Inherited metabolic diseases

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13
Q

what is the most common inherited cause of learning disability

A

Fragile X syndrome

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14
Q

features of someone with fragile x syndrome

A

long narrow face
prominent jaws
prominent ears

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15
Q

what is angelman syndrome

A

frequent laughter/smiling, happy demeanour, excitable, flappy hands

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16
Q

characteristics of goldenhar syndrome

A

hemi facial microsomia (half of face is smaller)
cleft lip and palate

17
Q

characteristics of teacher collins syndrome

A

hypoplasia of mid face structures
skeletal class ii
visual impairment
cleft palate
AOB
spacing
hypodontia

18
Q

characteristic of Pierre robin syndrome

A

micrognathia (retruded mandible)
glossoptosis
cleft palate

19
Q

what syndrome exclusively affects females

A

Turner syndrome

20
Q

what is sturge weber

A

congenital neurological and skin condition
skin: facial haemangioma

21
Q

aetiology of cleft lip and palate

A

genetic and environmental

22
Q

associated dental anomalies with cleft lip and palate

A

class III skeletal
hypodontia
supernumeries
size and shape abnormalies
delayed eruption
hypomineralisation

23
Q

what is spine bifida

A

babies spine and spinal cord does not develop properly

24
Q

what is hydrocephalus

A

water in the brain

25
considerations for patient with transplants
treat as high caries risk treat all active disease prior to transplant liaise with medical teams cyclosporin and tacrolimus medication
26
presentation of graft versus host disease
lichenoid appearing hyperkeratotic erythema
27
what is premature loss of primary teeth a clinical concern
age 3
28
characteristics of hypophospotasia
bone fracturse exfoliation of teeth reduced dentine enlarged pulp chambers
29
characteristic of papillon fefevre syndrome
palmar plantar hyperkeratosis severe inflammation and degeneration of periodontal tissues
30
who are Glass children
children that have siblings with a chronic illness