Childhood development Flashcards

1
Q

Failure to thrive

A

Poor physical growth and development in a child.

Faltering growth- children fall in weight across:
- One or more centile spaces if their birthweight was below the 9th centile

  • Two or more centile spaces if their birthweight was between the 9th and 91st centile
  • Three or more centile spaces if their birthweight was above the 91st centile
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2
Q

causes of failure to thrive

A

inadequate energy and nutrition can lead to failure to thrive:

Inadequate nutritional intake
- maternal malabsorption, iron deficiency anaemia, neglect, family/parental problems, poverty.

Difficulty feeding
- poor suck (cerebral palsy), cleft lip/palate, genetic conditions, pyloric stenosis

Malabsorption
- CF, coeliac disease, cows milk, chronic diarrhoea, IBD

Increased energy requirements
- hyperthyroidism, congenital heart disease, CF, malignancy, HIV/immunodeficiency

Inability to process nutrition

  • inborn errors of metabolism
  • type 1 diabetes
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3
Q

assessment of failure to thrive

A

Pregnancy, birth, developmental and social history
Feeding or eating history
Observe feeding
Mums physical and mental health
Parent-child interactions
Height, weight and BMI (if older than 2 years) and plotting these on a growth chart
Calculate the mid-parental height centile

mid parental height (height of mum + height of dad) / 2

BMI = weight (kg) / height m2

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4
Q

investigations for failure to thrive

A

urine dipstick (UTI)
coeliac screen (anti TTG, anti eMA)
CF
pyloric stenosis

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5
Q

causes of short stature

A

a height more than 2 standard deviations below the average for their age and sex. This is the same as being below the 2nd centile.

Familial short stature
Constitutional delay in growth and development
Malnutrition
Chronic diseases, such as coeliac disease, inflammatory bowel disease or congenital heart disease
Endocrine disorders, such as hypothyroidism
Genetic conditions, such as Down syndrome
Skeletal dysplasias, such as achondroplasia

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6
Q

normal reflexes

A
  1. the moro reflex= baby is startled by loud sound / movement. lasts 2 months old. baby cries, throws back head and pulls limb into body
  2. the tonic reflex (fencing)
    baby is turned to one side, and the same arm stretches out whilst hte opposite arm bends at elbow. lasts 5-7 months
  3. rooting reflex
    stroke corner of baby’s mouth. baby turns head and opens mouth. lasts 4 onths
  4. suck reflex. roof of baby’s mouth is touched = baby starts to suck, (premature babies will have a weak or immature suckling ability)
  5. grasp reflex. stroke palm of baby’s hand- baby will close their fingers. 5-6 months.
  6. stepping reflex. 2 months. baby takes steps when held upright.
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7
Q

senses

A

sight: unco-ordinated eye movement, focus only at close range (8-10 inches) can track an object. improves to 20/20 in first 2-3 years. can detect light and dark but not colours
hearing: fully developed in newborns. startles to loud noises. prefer higherp itch voice
smell: strong sense of smell, prefers smell of mum and breast milk
taste: sweet taste, human milk
touch: comforted by touch

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8
Q

Gross motor development

A

4 months: able to support their head and keep it in line with the body

6 months: keep their trunk supported on their pelvis (i.e. maintain a sitting position)

9 months: sit unsupported by 9 months. crawling at this stage

**refer if unable to sit supported at 12 months
12 months: cruising (walking whilst holding onto furniture).

15 months: Walk unaided.

**refer if unable to stand independently by 18 months

18 months: Squat and pick things up from the floor.

2 years: Run. Kick a ball.

  • **refer if unable to walk independently at 2 years
  • **refer if unable to run at 2.5 years

3 years: Climb stairs one foot at a time. Stand on one leg for a few seconds. Ride a tricycle.
4 years: Hop. Climb and descend stairs like an adult.

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9
Q

fine motor development

early milestones

A

8 weeks: Fixes their eyes on an object 30 centimetres in front of them and makes an attempt to follow it. preference for a face rather than an inanimate object.

6 months: Palmar grasp of objects (wraps thumb and fingers around the object).

*** refer if at 5 months not able to hold an object at 5 months

9 months: Scissor grasp of objects (squashes it between thumb and forefinger).

12 months: Pincer grasp (with the tip of the thumb and forefinger).

14-18 months: They can clumsily use a spoon to bring food from a bowl to their mouth.

hand preference before 12 months is abnormal and could indicate cerebral palsy

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10
Q

emotional and social development

A

6 weeks: Smiles

3 months: Communicates
pleasure

6 months: Curious and engaged with people

9 months: They become cautious and apprehensive with strangers

12 months: Engages with others by pointing and handing objects. Waves bye bye. Claps hands.

18 months: Imitates activities such as using a phone
***refer if no words at 18 months and no interest in others.

2 years: Extends interest to others beyond parents, such as waving to strangers. Plays next to but not necessarily with other children (parallel play). Usually dry by day.

3 years: They will seek out other children and plays with them. Bowel control.

4 years: Has best friend. Dry by night. Dresses self. Imaginative play.

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11
Q

hearing and vision

A
newborn: startled by sudden noise
1m startled by loud noise
3m moves head to gaze
6m adjust to see and turns to sound
12m good vision, knows name
18m self in mirror
2y/o interested in conversation
30m photos
4y/o colours, long stories
5 y/o 10 colors
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12
Q

speech and language development

A

expressive:
3 months: Cooing noises
6 months: Makes noises with consonants (starting with g, b and p)
9 months: Babbles, sounding more like talking but not saying any recognisable words
*refer if not babbling or imitating sounds by the age of 9 months.

12 months: Says single words in context, e.g. “Dad-da” or “Hi”
*refer if does not respond to own name by 1 year old

18 months: Has around 5 – 10 words

2 years: Combines 2 words. Around 50+ words total.
**less than ten spoken words by the age of 2 is indicative of ASD.

2.5 years: Combines 3 – 4 words
3 years: Using basic sentences
4 years: Tells stories

receptive:
3 months: Recognises parents and familiar voices and gets comfort from these
6 months: Responds to tone of voice
9 months: Listens to speech
12 months: Follows very simple instructions
18 months: Understands nouns, for example “show me the spoon”
2 years: Understands verbs, for example “show me what you eat with”
2.5 years: Understands propositions (plan of action), for example “put the spoon on / under the step”
3 years: Understands adjectives, for example “show me the red brick” and “which one of these is bigger?”
4 years: Follows complex instructions, for example “pick the spoon up, put it under the carpet and go to mummy”

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13
Q

fine motor
drawing skills
tower of bricks
pencil grasp

A
drawing:
12 months: Holds crayon and scribbles randomly
2 years: Copies vertical line
2.5 years: Copies horizontal line
3 years: Copies circle
4 years: Copies cross and square
5 years: Copies triangle
towers:
14 months: Tower of 2 bricks
18 months: Tower of 4 bricks
2 years: Tower of 8 bricks
2.5 years: Tower of 12 bricks
3 years: Can build a 3 block bridge or train
4 years: Can build steps

pencils:
Under 2 years: Palmar supinate grasp (fist grip)
2-3 years: Digital pronate grasp
3-4 years: Quadruped grasp or static tripod grasp
5 years: Mature tripod grasp

3 years: Can thread large beads onto string. Can make cuts in the side of paper with scissors.
4 years: Can cut paper in half using scissors

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14
Q

learning disability

A

different conditions that effect ability of a child to develop new skills. mild-severe

Dyslexia refers to a specific difficulty in reading, writing and spelling.

Dysgraphia refers to a specific difficulty in writing.

Dyspraxia, also known as developmental co-ordination disorder, refers to a specific type of difficulty in physical co-ordination. It is more common in boys. It presents with delayed gross and fine motor skills and a child that appears clumsy.

Auditory processing disorder refers to a specific difficulty in processing auditory information.

Non-verbal learning disability refers to a specific difficulty in processing non-verbal information, such as body language and facial expressions.

Profound and multiple learning disability refers to severe difficulties across multiple areas, often requiring help with all aspects of daily life.

IQ:
55 – 70: Mild
40 – 55: Moderate
25 – 40: Severe
Under 25: Profound
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15
Q

reasons for developmental delay

A
global developmental delay
(in all developmental domains)
- down's syndrome
- fragile X
- fetal alcohol syndrome
- Rett syndrome
- Metabolic disorders
Gross motor delay
Cerebral palsy
Ataxia
Myopathy
Spina bifida
Visual impairment
fine motor delay
Dyspraxia
Cerebral palsy
Muscular dystrophy
Visual impairment
Congenital ataxia (rare)
language delay
Specific social circumstances, for example exposure to multiple languages or siblings that do all the talking
Hearing impairment
Learning disability
Neglect
Autism
Cerebral palsy

personal/social delay
Emotional and social neglect
Parenting issues
Autism

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16
Q

delayed puberty

A

normal:
girls 8-14
breast buds, pubic hair, menstrual periods

boys 9-15
enlargement of testicles then penis, gradual darkening of the scrotum, development of pubic hair, deepening of the voice

17
Q

tanner staging

A

determine the pubertal stage based on examiantion and findings of sex characteristics

18
Q

hypogonadism

A

lack of the sex hormones, oestrogen and testosterone, that normally rise prior to and during puberty.

lack of these hormones causes a delay in puberty.

Hypogonadotrophic hypogonadism: a deficiency of LH and FSH
Hypergonadotrophic hypogonadism: a lack of response to LH and FSH by the gonads (the testes and ovaries)

19
Q

hypogonadotropic hypogonadism

A

deficiency in LH and FSH
deficiency in testosterone and oestrogen

can be due to:
Previous damage to the hypothalamus or pituitary, for example by radiotherapy or surgery for previous cancer
Growth hormone deficiency
Hypothyroidism
Hyperprolactinaemia (high prolactin)
Serious chronic conditions can temporarily delay puberty (e.g. cystic fibrosis or inflammatory bowel disease)
Excessive exercise or dieting can delay the onset of menstruation in girls
Constitutional delay in growth and development is a temporary delay in growth and puberty without underlying physical pathology
Kallman syndrome

20
Q

hypergonadotropic hypogonadism

A

gonads cannot respond to stimulation by LH and FSH. no negative feedback from the sex hormones so the anterior pituitary gland increase the amount of LH and FSH produced.

Previous damage to the gonads (e.g. testicular torsion, cancer or infections, such as mumps)
Congenital absence of the testes or ovaries
Kleinfelter’s Syndrome (XXY)
Turner’s Syndrome (XO)

21
Q

Kallman syndrome

A

genetic condition causing hypogonadotrophic hypogonadism

failure to start puberty

associated with a reduced or absent sense of smell (anosmia).

22
Q

investigation for delayed puverty

A

history: fhx, diet, lifestyle
height, weight, pubertal development

Full blood count and ferritin for anaemia
U&E for chronic kidney disease
Anti-TTG or anti-EMA antibodies for coeliac disease
Hormonal blood tests can be used to look for hormonal abnormalities:

Early morning serum FSH and LH (the gonadotropins). These will be low in hypogonadotrophic hypogonadism and high in hypergonadotrophic hypogonadism.
Thyroid function tests
Growth hormone testing. Insulin-like growth factor I is often used as a screening test for GH deficiency.
Serum prolactin
Genetic testing with a microarray test can be used to look for underlying genetic conditions:

Kleinfelter’s syndrome (XXY)
Turner’s syndrome (XO)
Imaging can be useful:

Xray of the wrist to assess bone age and inform a diagnosis of constitutional delay
Pelvic ultrasound in girls to assess the ovaries and other pelvic organs
MRI of the brain to look for pituitary pathology and assess the olfactory bulbs in possible Kallman syndrome