Growth & Development Flashcards

1
Q

What are the normal growth patterns in infants

A

0-6 months: 2cm every month and 170g every week
6-12 months: 1cm every month and 110g every week

First week will lose 5-10% of birth weight but should be double by 4-5 months
Fontanelles close between 10-24 months
Preterm age calculated by total age - (40 weeks - actual gestation)

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2
Q

Discuss the definitions of age and two predicted height methods

A

Chronological age
Height age: age at which height it at 50th percentile
Bone age: skeletal maturation which reflects residual growth potential by assessing growth plates in hands

Target Height:
boys = (Father’s height + Mother’s height +13)/2
Girls = (Father’s height + Mother’s height -13)/2

Predicted Height:
- estimated based on chronological and bone age

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3
Q

What are the criteria for failure to thrive?

A
  • weight for age <3rd percentile
  • weight for length <3rd percentile
  • cross 2 major percentile lines
  • weight <80% ideal weight for age (weight same percentile as height percentile)
  • infant not gaining weight despite sufficient intake
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4
Q

What are the timings for puberty in girls and boys

A

Girls: 8-13
Boys: 9-14

Girls reach peak height velocity 2 years earlier

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5
Q

What is the physiology of puberty?

A

Hypothalamus secretes GnRH stimulating pituitary to release LH and FSH (usually greatest during sleep) -> LH and FSH lead to gonads to grow and secrete testosterone (males) or estrogen and progesterone (females) -> sex hormones lead to puberty changes (testosterone cause hair growth in both and growth spurt in males and estrogen leads to breast development and growth spurt)

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6
Q

Discuss the sequence of puberty changes in boys and girls

A

Girls: boobs, pubs, grow and then flow (though adult breasts and pubic hair occur following menarche)
Boys: testis enlargement -> pubic hair -> penis growth -> peak height velocity -> adult genital and then adult pubic hair

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7
Q

What does the Denver Development Screening tool assess

A

Social contact
Fine motor skills
Language
Gross motor

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8
Q

What is short stature?

A

> 2SD below mean height based on sex and age
Height is assessed when:
- low growth rate of <5cm/year
- downward crossing of percentiles after age of 18 months
- height below 3rd percentile
- height significant below target height percentile

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9
Q

Discuss the approach to short stature

A

Child following percentile on growth and weight, with height in target height percentile:

  • constitutional delay where normal growth velocity following percentile for age >3 (retarded before then), delayed bone age, delayed pubertal maturation, family history
  • familial short stature: normal growth velocity following percentile for age >3, normal bone age, family history

Pathologic when have abnormal proportions (upper to lower body ratio should be 1.7 at birth, 1.3 at 3 and 1.0 at 8 or if arm to height ratio is greater than 5cm or 4%)
- marker of skeletal dysplasia: Prader-Willi, Turner, Down’s, achondrodysplasia (high upper to lower segment ratio)

Normal proportions assess 0-3 growth and 2-17 growth

  • prenatal abnormal growth due to IUGR or genetic syndrome
  • postnatal abnormal growth due to malnutrition, chronic disease, medication (glucocorticoids), endocrinopathy

Increased weight for height ratio pathological growth:
- endocrinopathy due to growth hormone deficiency: IGF-1 resistance, hypothyroidism, glucocorticoid excess, poorly controlled diabetes

Decreased weight for height ratio (both are low):
- malnutrition or systemic disease

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10
Q

Discuss the differential for failure to thrive

A
Inadequate caloric intake:
- food insecurity
- inappropriate feeding technique
- mood or eating disorder
- cardiopulmonary disease or GI disorder
- difficulty eating (cleft palate or GERD)
Inadequate absorption:
- cow's milk protein allergy
- IBD
- celiac
- GI obstruction
Excessive metabolic demand
- hyperthyroidism
- malignancy
- JIA
- chronic respiratory or heart disease
Defective utilization of nutrients:
- inborn errors of metabolism
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11
Q

Discuss the outpatient and inpatient management of failure to thrive

A
Outpatient:
- increased caloric intake for catch up growth
- limit empty calories
- 3 meals a day with snacks in between
- structured mealtimes
- offer solids before liquids
Inpatient:
- fail outpatient
- concern for safety
- risk of refeeding syndrome
- nasogastric tube feeding
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12
Q

List some major developmental milestones

A

2 months: head control -> hold head up in sitting at 4 months
6 months: transfer object to hand and sits well unsupported
8 months: stand with assistance
1 year:
- pincer grip by 10 months and stacking cubes
- walks
- 1st word, 10 words by 1 year
2 years:
- 2 word sentences, uses crayons, goes down stairs
4 years:
- copies rectangle, self grooms
- tells stories and compound sentences

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13
Q

Discuss the definition of intellectual disability

A

Deficit in both intellectual and adaptive functioning before age of 18

  • intellectual: low IQ
  • adaptive: limitations to conceptual, social and practical

Global developmental delay: below age 5 who fail to meet milestones in >=2 areas of intellectual functioning

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14
Q

Discuss the definition of cerebral palsy and the early signs

A

Non-progressive syndromes characterized by motor and postural dysfunction due to abnormal neurodevelopment

  • early after birth have dyskinetic movements or later due to abnormal posture, abnormal movement and not meeting motor development
  • motor is uncoordinated, stereotypic and limited in cerebral palsy
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15
Q

What are the syndromes of cerebral palsy

A

Spastic syndromes:
- positive signs of spastic hyperteonia (velocity dependent increase in tone) and hyper-reflexia
- negative slow effortful voluntary movements, impaired fine motor control
Dyskinetic syndromes
Ataxic syndromes

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16
Q

What is the differential for developmental delay

A

Genetic syndromes: Downs and Fragile X
CNS Cause: TORCH, meningitis, structural
Metabolic
Environmental

17
Q

What are red flags for developmental delay

A
Gross motor:
- delay in disappearance of primitive reflexes
- abnormal movement patterns
- no head control by 3-4 months
- no independent sitting by 8-9 months
- no steps by 18 months
Fine motor:
- fisting hands >50% of time by 4 months
- not reaching for objects by 6 months
- hand dominance earlier than 18 months
Language:
- no attempt at words by 18 months
- Lower than expected language milestones
18
Q

What is delayed puberty

A

No breast development by age 12 in girls

No increase in testicular size by 14 in boys

19
Q

Discuss the approach to delayed puberty

A

Primary Hypogonadism or Hypergonadotropic Hypogonadism: high FSH and LH
- gonadal failure due to chromosomal abnormality or therapy/infection affecting the gonads
Secondary Hypogonadism or Hypogonodotropic Hypogonadism: Low FSH and LH
- failure of pituitary gland due to constitutional delay, decreased nutrition or high metabolic demand, CNS tumour or infiltrative disease

20
Q

Discuss the treatment for delayed puberty in girls and boys

A

Girls:
- estrogen increase over 1-2 years and then add progesterone when begin menstruating
Boys:
- testosterone IM injection
- LH and FSH would be needed for teste growth and fertility

21
Q

When do the primitive reflexes disappear?

A

4-6 months

22
Q

What are some of the postural reflexes and when do they appear?

A
Head righting (4 months): keep head midline even when tilting to side
Frontal Propping (5-6m)
Lateral propping (7-8m)
Backward propping (10-12m)
23
Q

How many kcals per ounce does breast milk have

A

20kcal/oz or 0.7kcal/mL (30mL/oz)

Require 100-125 in 0-1month
Require 95-100 in 1-12 month
Require 80-100 in 1-3 year

24
Q

Describe encopresis

A

Is fecal incontinence that is repetitive, voluntary or involuntary, passage of stool in inappropriate places by children 4 years of age or older

  • may have associated constipation
  • due to constipation can have abnormal bladder function as well
25
Q

Discuss dysfunctional voiding

A
  • occurs when there is detrusor contraction against a closed external urethral sphincter due to inability to relax sphincter during voiding
  • may have associated spinal cord lesion
  • if non-neurological cause have increased risk of constipation, encopresis and subsequent VUR and renal scarring
26
Q

Discuss the presentation of tethered cord syndrome

A
Pathophysiology:
- filum terminale is attached to inelastic structure caudally resulting in stretch induced dysfunction
Presentation
- toddlers and children
- motor and sensory dysfunction
- loss of bladder control
27
Q

What are the differences between:
Monosymptomatic nocturnal enuresis
Nonmonosymptomatic nocturnal enuresis

A

Monosymptomatic nocturnal enuresis
- enuresis with no history of LUT symptoms and without history of bladder dysfunction
Nonmonosymptomatic nocturnal enuresis
- children that do not fit MNE criteria
- LUT symptoms, daytime wetting, encopresis

28
Q

Discuss the role of the sympathetic and parasympathetic nervous systems in micturition

A

Sympathetic: Store urine
- T11-L2 relax detrusor muscle
- contract internal urethral sphincter via alpha-adrenergic receptors
Parasympathetic - Release urine
- S2-S4 contract the bladder
- Somatic S2-S4 relaxation of the external urethral sphincter and pelvic floor musculature