Familial Short Stature and SGA ✅ Flashcards

1
Q

What is the most common cause of short stature referred to clinical services?

A

Familial short stature

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2
Q

What is required to demonstrate familial short stature?

A

Calculating the target height range

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3
Q

What should be considered if one parent is particularly short?

A

If they too have a potentially inheritable underlying growth disorder

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4
Q

What will children with familial short stature show in their growth chart?

A

Height centile consistent with their short target height range, and growth parallel to the centiles and consistent with a normal height velocity

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5
Q

How is familial short stature managed?

A

Careful explanation and reassurance for the child and parents

Extensive investigation not indicated

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6
Q

When is short stature due to being small for gestational age suggested?

A

When the birth weight is below the 10th centile

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7
Q

What does symmetrical growth failure in utero suggest?

A

Adverse influences on fetal growth that have operated throughout much of development

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8
Q

What is meant by asymmetrical growth?

A

When head circumference is preserved

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9
Q

What does asymmetrical growth failure in utero suggest?

A

Growth failure restricted to the last part of pregnancy, often placental failure

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10
Q

What % of SGA infants will show catch-up growth postnatally?

A

80-85%

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11
Q

Are infants with symmetrical or asymmetrical intrauterine growth resection more likely to show catch-up growth postnatally?

A

Asymmetrical

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12
Q

What are SGA infants at higher risk of in the first 2 days of life?

A

Hypoglycaemia

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13
Q

What are SGA infants at higher risk of longer term?

A

A range of adult diseases, including hypertension, cardiovascular disease, T2DM, and obesity

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14
Q

What has been proposed to explain why SGA foetuses are at higher risk of certain adult diseases?

A

The Barker hypothesis

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15
Q

What is the Barker hypothesis?

A

That there are critical periods in fetal development where permanent adaptive changes occur in body structure and function to cope with nutritional insufficiency in utero and likely nutritional challenges postnatally. However, these adaptations place the individual at a disadvantage postnatally should calorie supplies become potentially unlimited.

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16
Q

What does treatment of infants with SGA involve?

A

Ensuring adequate supply of nutrition postnatally to facilitate catch up growth

17
Q

How can SGA infants that remain short be managed?

A

GH therapy at larger doses than required to treat GH deficiency - has been shown to increase final height

18
Q

Does GH therapy for SGA infants impact on other risk factors for disease later in life?

A

Unknown