Professional Documents
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BMI-for-Age
Weight-for-Length < 5th Underweight
Head Circumference- for-Age < 5th and > 95th Developmental Problems
35 35
95th
95th
30 30
50th
25
Weight (kg)
5th
25
20 50th
BMI
15 20 5th
10
15
5
0 10
80 90 100 110 120 130 24 72 120 168 216
Stature (cm) Age (months)
For Children, BMI Changes with Age
BMI BMI
Age BMI
2 yrs 19.3
4 yrs 17.8
9 yrs 21.0
13 yrs 25.1
BMI BMI
Can you see risk?
Risk factors/etiology:
•Pathologic (postnatal onset)
•Constitutional growth delay
•Familial short stature
•Prenatal onset short stature (IUGR)
Presentation:
Pathologic :
Starts with the patient in the normal range for
height
Over time, starts falling off the height curve,
crossing percentiles
Constitutional:
Starts with the patient in the normal range for
height
Over time, normal final adult height is reached ,
but the growth spurt and puberty are delayed
Causes of short stature
A. Genetic-familial short stature
B. Constitutional growth delay
C. Endocrine disturbances
1. Growth hormone deficiency
2. Hypothyroidism
3. Excess cortisol—Cushing disease and Cushing
syndrome (including iatrogenic causes)
4. Precocious puberty
5. Diabetes mellitus (poorly controlled)
6. Pseudohypoparathyroidism
7. Rickets
Causes of short stature (contd…)
D. Intrauterine growth restriction
1. Intrinsic fetal abnormalities—chromosomal disorders
2. Syndromes (eg, Noonan )
3. Congenital infections
4. Placental abnormalities
5. Maternal abnormalities
a. Hypertension/toxemia
b. Drug use
c. Malnutrition
Causes of short stature (contd…)
E. Inborn errors of metabolism
1. Mucopolysaccharidosis
2. Other storage diseases
F. Intrinsic diseases of bone
1. Defects of growth of tubular bones or spine (eg,
achondroplasia)
2. Disorganized development of cartilage and fibrous
components of the skeleton (eg, multiple cartilaginous
exostoses, fibrous dysplasia with skin pigmentation)
Causes of short stature (contd…)
G. Short stature associated with chromosomal
defects
1. Autosomal (eg, Down syndrome, Prader-Willi
syndrome)
2. Sex chromosomal (eg, Turner syndrome-XO)
H. Chronic systemic diseases, congenital defects,
and cancers (eg, chronic infection and infestation, IBD,
hepatic disease, CVS disease, hematologic disease, CNS
disease, pulmonary disease, renal disease, malnutrition,
cancers, collagen vascular disease)
I. Psychosocial short stature (deprivation
dwarfism)
Familial:
Stays parallel to the growth curve
Strong family history of short stature
Treatment:
•Correction of the underlying disease state
•Growth hormone in selected cases
D/D:
Work-up for short stature
•Familial: A normal variant,
•Exogenous obesity
•Endocrine: growth hormone excess (gigantism,
acromegaly)
•Androgen excess (tall as children but short as
adults)
•Hyperthyroidism
•Genetic syndromes metabolic disorders:
homocystinuria, cerebral gigantism , Beckwith-
Wiedemann, Weaver-Smith, and Klinefelter
syndrome
A. Constitutional (familial)
B. Exogenous obesity
C. Endocrine causes
1. Growth hormone excess (pituitary
gigantism)
2. Precocious puberty
3. Hypogonadism
D. Nonendocrine causes
1. Klinefelter syndrome
2. XYY males
3. Marfan syndrome
4. Cerebral gigantism (Soto syndrome)
Homocystinuria:
•Autosomal recessive
•Incidence 1:200,000
•Marfanoid appearance
•mental retardation or psychiatric illness
Treatment
Exercise and a balanced diet
Complications:
•Increased risk for becoming obese adults
•Cardiovascular (HTN, increased cholesterol)
•Hyperinsulinism
•Slipped capital femoral epiphysis
•Sleep apnea
D/D:
•Endocrine causes (Cushing, hypothyroidism,
Prader-Willi)
•Genetic causes (Turner, Laurence-Moon-Biedl)