Evaluation of Worrisome Growth Flashcards

1
Q

3 height definitions worrisome growth

A
  1. short stature: below -2SD for age and gender or height more than 2SD below mid parental height target
  2. dwarfism: below -3SD for age
  3. Midget: dwarf with normal body proportions
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2
Q

worrisome growth velocity

A

abnormally slow linear growth velocity or dropping across two major gentile lines on the growth chart

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3
Q

genetic potential formula

A

Boys:
.5[mother’s height + 13cm(5in) + father’s height]

Girls:
.5[father’s height - 13cm(5in) + mother’s height]

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4
Q

The degree of skeletal maturation is directly correlated with what?

A

time of epiphyseal closure

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5
Q

body proportions at birth vs 10yearsold

A

upper to lower body ratio

birth: 1.7
10years: 1.0

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6
Q

Arm span boys vs girls

A

boys: shorter than height before 10-11 years; average adult male arm span 5.2cm>ht
girls: shorter than height before 10-14 years; average adult female arm span 1.2cm>ht

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7
Q

constitutional growth delay definition

A

growth deceleration during first 2 years of life followed by normal growth and paralleling lower percentile curve throughout prepubertal years

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8
Q

constitutional growth delay characteristics

A
  1. delayed skeletal maturation
  2. catch up growth during late puberty and delayed fusion of growth plates
  3. end result: lower end of normal height for families
  4. polygenic trait; positive family in about 60-80% of patients
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9
Q

treatment of growth delay characteristics

A

normal growth pattern

boys >11 with testosterone to avoid compromising final height

girls with estrogen

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10
Q

familial short stature

A

children have normal growth velocity and height wnl for parent’s height

initially will have decrease in growth rate between 6 and 18 mnths of age

some families may have tubular bone alterations: brachydactyl syndromes, SHOX haploinsufficiencies

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11
Q

failure to thrive

A

infants or young children with

1. deceleration of weight gain to a point

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12
Q

nutritional growth retardation

A

linear growth stunting from poor weight gain in children under 2years of age

may be secondary to systemic illnesses like celiac, iBD
stimulant medications

sometimes hard to distinguish from constitutional growth delay and constitutional thinness

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13
Q

small for gestational age (SGA)

A

less than -2SD for birth weight or length

etiologies:

  1. maternal: infection, nutritional deficiencies, uterine abnormalities, smoking, ETOH, drugs
  2. Placental: previa, abruption, infarcts, structural, multiple gestation
  3. fetal: chromosomal abnormalities, metabolic, infections, malformations
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14
Q

Catch up growth and final height in SGA

A

most healthy infants achieve catch up height by age 2 years; most of which is achieved within 6 months of birth

10-15% of children born SGA will remain short as adults

final height can also be compromised by early puberty

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15
Q

GH treatment in SGA children

A

SGA children who have catch up growth by 2 years

GH should not be given without appropriate nutritional intake

may increase final height by an average of 3 inches: -1.1–> -0.9 SD from -2.3 SDS

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16
Q

4 hormonal causes of worrisome growth

A
  1. hypothyroidism
  2. growth hormone/ IGF-1 abnormalities
  3. Cushing syndrome
  4. Rickets
17
Q

hypothyroidism in children

A

profound growth failure

many clinical features seen in hypothyroid adults not seen in children

18
Q

primary vs central hypothyroidism

A

primary: increased TSH, low T4

Central: low T4, normal TSH

19
Q

growth hormone

A

anterior pituitary hormone

promotes linear growth

affects body composition to increase lean body mass and decreases fat

20
Q

6 reasons for congenital growth hormone deficiency

A
  1. hypothalamic pituitary malformations
  2. holoprosencephaly/ schizencephaly
  3. isolated cleft lip or palate
  4. Septo-Optic Dysplasia: 50% have hypopituitarism
  5. Optic nerve hypoplasia
  6. Empty sella syndrome
21
Q

5 reasons for acquired GH deficiency

A
  1. trauma
  2. CNS infection
  3. CNS tumors
  4. cranial irradiation
  5. hypophysitis
22
Q

growth hormone deficiency on the graph

A

abnormal growth velocity with exclusion of other causes

23
Q

7 GH Deficiencies signs

A
  1. decreased muscle build
  2. increased SubQ fat
  3. Immature face for age
  4. Prominent forehead, depressed midface
  5. small phallus in males
  6. other midline facial defects
  7. history of prolonged jaundice and or hypoglycemia in newborn period
24
Q

growth hormone deficiency evaluation 3 parts

A
  1. bone age
  2. IGF-1 (IGFBP-3 in infant): however low in underweight children regardless of GH status
  3. Stimulation testing (never draw random GH level): clonidine, arginine, glucagon, l-dopa
25
Q

4 syndromic short stature reasons

A
  1. skeletal dysplasias and other genetic syndromes
  2. turner: haploinsufficiency of SHOX genes
  3. Prader-Willi: GH deficient
  4. Noonan: abnormal GH post receptor signaling
26
Q

turner syndrome stats

A

most common chromosome abnormality of females

~3% female concepti

complete of partial absence of 1 X chromosome

1/2000 live born females

27
Q

turner syndrome height

A

final height is about 20cm less than target if untreated

haploinsufficiency of SHOX genes responsible for skeletal and growth abnormalities

28
Q

turner syndrome height treatment

A

GH therapy improves growth and adult height despite the fact that they are usually not deficient

starting treatment early is important to offer best potential for growth

29
Q

4 skeletal abnormalities in Turner Syndrome

A
  1. short
  2. increased carrying angle
  3. short neck
  4. micro or retinognathia
30
Q

7 general abnormalities Turner syndrome

A
  1. cardiac abnormalities: bicuspid aortic valve, coarctation
  2. Renal: horseshoe kidney
  3. Ovarian insufficiency
  4. hypothyroidism/ celiac disease
  5. otitis media
  6. hearing loss
  7. non verbal learning disability
31
Q

3 lymph obstruction in turner

A
  1. low hairline
  2. webbed neck
  3. lymphedema
32
Q

3 categories to evaluate worrisome growth

A
  1. bone age: left hand and wrist
  2. screening labs: metabolic pannel, CBC, UA, karyotype in girls, TSH & T4 (IGF-1)
  3. Nutritional growth retardation: ESR, TTG, IgA