Introduction to growth Flashcards

1
Q

What should babies and toddlers wear when being weighed?

A

babies naked
toddlers in vest and pants, no shoes

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2
Q

What is used to measure height?

A

stadiometer

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3
Q

How do you describe changes in a child’s height or weight over time?

A

falls or rises should be expressed as multiples of centiles spaces from a growth chart
eg. a fall of 2 centile spaces

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4
Q

Target height calculation for a boy

A

(mother’s height + father’s height +13)/2

mid-parental height +/-5

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5
Q

Target height calculation for a girl

A

(mother’s height + father’s height -13)/2

mid-parental height +/-5

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6
Q

Normal childhood growth phases

A

3 phases

infancy = most rapid growth phase
mid-childhood = 5-7cm/year, no difference between males and females
puberty = males start puberty later and have a larger growth spurt

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7
Q

List some causes of short stature

A

congenital hypothyroidism
juvenile hypothyroidism
growth hormone deficiency
Turner’s syndrome
familial short stature
Cushing’s syndrome
Prader-Willi syndrome

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8
Q

When would you be more concerned short stature is down to a hormone problem?

A

if height is more affected than weight
eg. relatively normal weight gain

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9
Q

Prognosis of late-detected congenital hypothyroidism

A

cretinism
irreversible mental handicap

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10
Q

What tests should be done in suspected growth hormone deficiency?

A

growth hormone + GnRH test
cranial MRI (looking at pituitary

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11
Q

When does the pituitary gland develop?

A

6 weeks gestation

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12
Q

Why can’t you measure growth hormone randomly?

A

produced in peaks overnight

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13
Q

Growth hormone deficiency features

A

truncal adiposity
mid facial hypoplasia
neonatal jaundice
hypoglycaemia

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14
Q

Turner’s syndrome features

A

high palate
small hands
hypoplastic ridged nails
increased carrying angle

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15
Q

Turner’s syndrome karyotype

A

45XO/46XX

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16
Q

FSH and LH in Turner’s syndrome

A

high
due to premature ovarian failure

17
Q

Turner’s syndrome treatment

A

growth hormone
oestrogen

18
Q

Familial short stature features

A

current height centile = genetic centile
bone age = chronological age
no need for treatment
normal pubertal age

19
Q

Describe constitutional delay in growth

A

short stature - generally after 1-2 y of age
normal growth velocity, lower end
bone age = height age = delayed bone age
associated with delayed but normal puberty
may need pubertal induction with testosterone at appropriate age

20
Q

Cushing’s syndrome features in children

A

central obesity
growth failure
hypertension
psychological effects

21
Q

Causes of Cushing’s syndrome in children

A

ACTH dependent:
- pituitary
- ectopic ACTH

Adrenal tumour

22
Q

Prader-Willi syndrome features

A

infantile hypotonia
insatiable appetite
short stature
subtle dysmorphic features
moderate learning disability
behaviour problems

23
Q

Genetic cause of Prader-Willi syndrome

A

paternal 15q11 deletion

24
Q

What would suggest androgen exposure in a baby/child?

A

body odour
pubic/axillary hair
no breast development

[normal puberty = breast buds develop first]

25
What hormone is high in congenital adrenal hyperplasia?
17 alpha hydroxyprogesterone
26
What causes congenital adrenal hyperplasia?
21 hydroxylase deficiency 11 beta hydroxylase deficiency 17 hydroxylase deficiency
27
Medical management of congenital adrenal hyperplasia?
hydrocortisone fludrocortisone sodium chloride (lots of salt loss occurs in this condition so needs replacing) monitor testosterone, 17OHP, growth, bone age, puberty