Evaluation of Worrisome Growth Flashcards

1
Q

CDC growth charts are based on _____

A

US population,

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2
Q

WHO growth charts are based on _____

A

world‐ wide population.

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3
Q

Short stature is defined as:

A

Height below -2 SD (3% is – 1.9 SD) for age and gender
or, a better option is
Height more than 3.5 inches below the midparental target height
*

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4
Q

_____ of children will fall within 3.5 inches of midparental target height

A

97%

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5
Q

How is Bone age measured ?

A

By comparing an X-ray of the left hand and wrist to standardized pictures of X-rays in a reference book.

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6
Q

children who have short parents are not necessarily born small, they will have a decrease in their growth rate between ______ of age to establish a new
trajectory

A

6 and 18 months

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7
Q

what is Constitutional Growth Delay?

A

(“Late Bloomer”)characterized by growth deceleration during the first 2 years of life, followed by normal
growth paralleling the lower percentile curve and shorter than expected for parental heights. Skeletal
maturation is delayed and catch-up growth is achieved by late puberty and delayed fusion of the
growth plates

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8
Q

what is the Definition of failure to thrive (FTT)

A

infant or toddler (< 2 years of age) with deceleration of weight gain to a point <3%, or a fall in weight across 2 or more major percentiles

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9
Q

what are Hormonal Causes of Worrisome Growth

Generally, weight is spared

A

 Hypothyroidism
 Growth hormone/IGF-1 deficiency
 Cushing Syndrome
 Rickets

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10
Q

Labs for Primary hypothyroidism should be ____

is straightforward

A

increased TSH, low T4

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11
Q

Labs for Central hypothyroidism

A

low T4, normal TSH

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12
Q

In primary hypothyroidism, pt will have a ___ bone age and __ face

A

delayed,

puffy (edematous)

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13
Q

Clinical findings in growth hormone deficiency:

A
Decreased muscle build
Increased subcutaneous fat, especially around trunk
Face immature for age
Prominent forehead, depressed midface
In males, small phallus
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14
Q

How to Evaluate for growth hormone deficiency:

A

1) Bone age (if child older than age 3 years)
2) IGF-1 can be helpful but has limitations:(May be reduced in malnutrition regardless of GH status,
IGFBP-3 is less affected by nutrition and may be a better test in very young children)
3)Stimulation testing – clonidine, arginine, glucagon, L-dopa (ruled out with any value >10 ng/ml)

Random, single GH value not useful, due to pulsatile secretion

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15
Q

The _____ gene is responsible for skeletal and growth abnormalities in turner syndrome

A

SHOX

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16
Q

Clinical findings of Turner syndrome

A
Cardiac abnormalities: bicuspid aortic valve, aortic coarctation
 Renal – horseshoe kidney
 Ovarian insufficiency
 Hypothyroidism/celiac disease
 Otitis media
 Sensory-neural hearing loss
 Non-verbal learning disability
17
Q

Side effects of GH treatment include ______

A

1) Slipped capital femoral epiphysis (fracture through the growth plate (physis), which results in slippage of the overlying end of the femur, )
2) Pseudotumor cerebri (idiopathic increase in ICP)