3. â˘Family seeks medical attention for their short child
Shorter than their younger sibling
â˘Shortest in their class
â˘Gets teased
â˘Bullied /treated differently in school
â˘Size not meet expectations
â˘Impediment to sports
â˘Want to be sure nothing WRONG
â˘SHORT STATURE CAUSING DISTRESS
â˘Severity of height deficit
â˘Degree of tolerance/ acceptance
â˘Childâs coping skills
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4. âHOW
TALL ARE YOU ?â instead of âWHAT IS YOUR
HEIGHTâ
Sandy allen (7ft ½ inch) never married
George W. Bush only the fourth major
presidential candidate to succeed over a taller
opponent
Girls referred half as boys and were significantly
shorter
Americans specialists prescribed 13x more GH to
boys for identical case scenarios
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5. ⢠Short stature imposes psychosocial
stress
⢠How short is too short ???
⢠Does short stature warrant medical treatment?
⢠A treatment approach based on suffering , rather than height ,
has been proposed
⢠CAUTION whether rhGH treatment for healthy short stature
children construes medical or cosmetic treatment
⢠Whether this is an appropriate means of resource allocation on a
societal level
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6. A child with growth retardation
⢠Height below 3rd percentile or -2SD to avg
population
⢠Excessively short for MPH/ target height
⢠GV <25th centile,not 3rd even if height is
within normal percentile
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8. NORMAL GROWTH VELOCITY
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Intrauterine pd is the pd. Of most rapid growth
1st year â 25cm
2nd year - 12.5 cm
3rd-4th year â 6-7 cm
5-9 year â 5 cm per year
Pre pubertal nadir â4 cm per year
Pubertal growth spurt 10-20 cms
Peak gain 10-12 cms boys, 7-9 cms girls
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9. ⢠Body proportion changes from 1.7 at birth to 0.98
â 1 by 13-14 years and to 1 in adulthood
⢠KEY to initial evaluation is
⢠history
⢠auxological parameters
⢠Detailed clinical examination
⢠Careful balance not to miss pathologIcal disorder
without over evaluation
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10. CAUSES OF SHORT STATURE
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Physiological short stature
familial
constitutional delay of growth and puberty
Pathological short stature
Systemic diseases
Chronic anaemia
Chronic renal failure
Chronic asthma
RTA
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congenital heart disease
chronic severe infection
malabsorption
chronic liver disease
Undernutrition
Psychosocial dwarfism
Endocrine disorders
growth hormone deficiency /insensitivity
hypothyroidism
cushing syndrome
pseudohypoparathyroidism
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Intrauterine growth retardation
Skeletal dysplasias and rickets
Genetic syndrome and enborn error of metabolism
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11. Facts to be elicited in history(etiology)
⢠Age at onset â since when the child is not
growing
⢠Previous growth records at school, home or
physician
⢠Records of previous height and weight must be
sought and charted on growth charts
⢠Ante natal history birthweight/gest.age/IUGR
⢠H/O birth asphyxia (hypopituitarism), breech
delivery, neonatal hypoglycemia, prolonged
neonatal hyperbilirubinemia(hypothyroidism)
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12. Symptoms pertaining to illness
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Shortness of breath, cyanosis, cough, fever,
Diarrhea, steatorrhoea, abdominal pain
Headache, vomiting, visual problems
Constipation, lethargy, feeding difficulty
Polyuria
H/O hepatitis , abdominal distention, malena
Recurrent blood transfusions
Dieatry history complementary feeding,
calculate calorie and protein intake
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13. ⢠Drug history prolonged use of corticosteroids
,amphetamine derrivatives
⢠Family history of SS in 1st/2nd degree relative
(FSS), delay in puberty in one or both
parent(CDGP)
⢠Social history , child abuse , family discord,
emotional deprivation (psychosocial
dwarfism)
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14. 1 -ANTHROPOMETRY
⢠Measurement is the basis of growth assessment
⢠accurate , precise and correctly interpreted
measurements are more specific than single
hormone assay
⢠Measurements should be accurate and
reproducible with <0.1% of coe. Of variation
⢠Appropriately designed equipment and
preferably by same person to eliminate
interpersonal errors
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15. Height
ďźFor children < 2 years : Supine length by
infanto meter , two person required
ďź> 2 years standing height by stadiometer
ďźPlot the value on a reference curve
ďźCalculate the height age
ďźCorrelate the height to MPH range in children
> 2 years
ďźTarget height range MPH+/- 8.5 cm
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16. 2- body proportions
⢠US:LS ratio- vertex to pubis :pubis to sole of foot
birth 1.7:1,3yrs 1.4:1,5yrs 1.3:1,6yrs 1.2:1,at 8 yrs
1.1:1, 10 yrs 0.98:1)
⢠LS longer than US >5 cms after puberty is
considered disproportinate
⢠Arm span /total height arm span is usually within
5 cm of height
⢠Weight, head circumference, and chest
circumference are the other parameters which
needs to be measured.
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24. BONE AGE
X ray left hand wrist to tips of fingers
ďź
TW3
ďź
GP ATLAS
ďź
GILSANZ and RATIB
x
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no . Of carpal bones
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25. WHY BONE AGE ?
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Skeletal maturity
Correlates closely with SMR
Speaks for remaining growth potential
Helps in adult height prediction
Delay of > 2 SD ie ~ 2 years is significant
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26. ESR
HOW TO INVESTIGATE
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?
SCREENING STAGE 1
Hemogram, ESR
LIVER and KIDNEY functions tests
Ca, phosph, alk. Phosph.
Antigliadin and transglutaminase antibodies
Karyotype in a girl and pelvic ultrasound
Thyroid function test
Bone age
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27. STAGE 2 SCREENING
⢠IGF- 1
⢠IGF binding protein 3( IGFBP-3)
⢠GROWTH HORMONE and other dynamic
stimulation test
⢠Neuro imaging
⢠Best to be done at SPECIALISED CENTRES
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28. child referred for growth retard.
anthropomettry growth charting , H/E
NORMAL
SHORT
CLUES TO ETIOLOGY FROM H/E
REASSURE AND ADVISE
ROUTINE HEIGHT AND WEIGHT
MONITOIRING YEARLY
absent
present
Bone
age
Confirmatory test
and treatment
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BL STATURE
N bone age
SIGNIFICA
NT
SHORT/
DELAYED
28
BA
29. SIGNIFICANT
SHORT,DELAYED BA
BL
OBSERVE GV FOR 1 YR
NORMAL
PHYSIOLGICAL
SS
REASSURE AND
ADVISE
GROWTH
MONITORING
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ABNORMAL
SCREENING
INVESTIGATIONS
ABNORM
AL
TREAT THE
CAUSE
NORMAL
KARYOTYPE IN GIRLS,TEST FOR GHD
,RTA, MALABSORPTION
ABNORMAL
NORMAL
TREAT CAUSE
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31. TAKE HOME MESSAGE
1
2
⢠Take height and weight properly and plot it
⢠Use growth charts (appropriate one)
⢠Growth velocity to be measured 6 monthly
⢠Systemic approach and simple test first
⢠DYNAMIC STIMULATION TESTS AT SPECIALISED CENTRES
3
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33. Familial short stature
⢠One of the MC cause of short stature
⢠Ht <3rd percentile but N against MPH
⢠GV normal, growth curve follows parallel to 3rd
centile line
⢠BA= HA, with N body proportion
⢠Child achieve puberty at appropriate age
⢠Adult stature is below normal
⢠Heritable causes of pathological short stature
with mild phenotype may actually responsible
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34. Constitutional delay of growth and
puberty (CDGP)
⢠More frequently encountered in boys
⢠Born with normal weight and length
⢠Grow normally in the 1st year, decelerates during
2nd -3rd year to reach just below 3rd cen
⢠Continue to grow parallel to 3rd percentile with
normal GV throughout the childhood
⢠Puberty delayed with growth spurt delayed and
attenuated
⢠BA=HA < CA
⢠H/O delayed puberty in either parent often
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