Child development

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4 Child development

Introduction

Understanding the pattern and time frame of normal development is an essential part of paediatric medicine. Whilst it is such an important building block in understanding children’s health, it may feel as though learning the sequence of early milestones is about as much fun as learning times tables at school. Like tables, however, a sound grasp of normal milestones is crucial when you are trying to make sense of child development.

Children follow a sequence of developmental skills. The age at which these skills are mastered can be compared within a large population of children, and normal ranges are described. This horizontal approach allows comparisons to be made with other children and is a good way of rapidly screening a population for those children who might be delayed.

For children who have delayed development it is important to compare the individual’s performance with their own previous performance (vertical assessment). This provides individual specific information about the rate of progress that will help to encourage and inform parents and professionals working with the child. Slowing in the rate of a child’s development is a worrying sign and may indicate a significant neurological disease.

In every developmental skill there may be differences in the quality of performance. Thus, most of us can kick a ball but, even with daily training, few of us could become a professional footballer. Certain skills are fundamental but as the tasks become more and more sophisticated, fewer individuals are able to acquire them.

Cross-sectional observation of many children at specific ages provides the basis of developmental tests such as the Denver Developmental Screening test, the Abilities of Babies and the Abilities of Young Children by Griffiths, the Bayley Scales of Infant Development and the Schedule of Growing Skills. Using these tests requires special training. All those working with children need to be able to perform an informal assessment of their development as outlined in this chapter.

Assessing an individual child’s development depends on:

Taking a history

The history can give a picture of a child that cannot always be obtained from observation so it is important to allocate sufficient time. It is a good idea to have a format so that you can make sure that important details are not missed. This is covered in Chapter 1. Particular areas of importance when considering a developmental disorder are detailed below.

The developmental milestones are best asked about in a systematic way:

The motor milestones

Play skills

Play skills develop rapidly in young children. Children who are uninterested in play should cause concern. The most common cause of loss of playfulness is that the child is unwell. However, a child who is said to be uninterested may be unable to play because of a physical difficulty or a learning difficulty. Another possibility is that the child has had limited play experiences and has been emotionally deprived.

Television is not an adequate substitute for playing with, and talking to, a baby.

The key milestones

There are three milestones, which, if not met, should ring ‘alarm bells’. These include:

Learning difficulty (mental retardation)

Learning difficulties are defined by IQ. A severe learning difficulty, as in the above case, is defined as an IQ of less than 35, moderate as an IQ of between 35 and 50, and mild as an IQ of between 50 and 70. The lower the IQ the more likely an organic explanation exists for the child’s difficulties. Increasingly, genetic causes of learning difficulties are being discovered. Inquire into alcohol use in pregnancy as fetal alcohol syndrome is a significant cause of mental retardation (see Chapter 18, page 266). A detailed family tree and questioning about the academic ability of relatives is useful; referral to a clinical geneticist may be of value, particularly if there are dysmorphic signs. Careful physical examination should seek any evidence of associated health problems and a careful search for dysmorphic features which might suggest a genetic problem. Investigation should be tailored to the individual case. See Table 4.1 for a list of tests, which should be considered.

Table 4.1 Investigations to be considered in a child with learning difficulties

Blood and urine tests
Full blood count and film
Haemoglobin electrophoresis
Thyroid function
ToRCH Screen
Creatine kinase
Uric acid
Calcium
Cholesterol
Low resolution micro-array (or Karyotype)
Specific genetic tests: Fragile X, MECP2 gene analysis, telomere analysis as indicated
Plasma and urine amino acids
Urine organic acids
Urine mucopolysaccharides
White cell enzymes
Acylcarnitines
Radiological investigations
Skull X-ray
MRI or CT scan
EEG
Retinal examination

Other common developmental disorders

Delay in bladder and bowel control

These problems are common and distressing. The key milestones to be concerned about are not being dry by the age of 7 years and soiling after the age of 4 years.

Nocturnal enuresis

Enuresis is defined as involuntary voiding of urine after the age of 5 years – most commonly at night – nocturnal enuresis (as in Case 4.5). By the age of 5 years, 93% of boys and 97% of girls are dry by day and night. By the age of 10 years, half of those with enuresis at the age of 5 years will be completely dry. If the child has previously been dry, the condition is described as secondary enuresis, and may be triggered by urinary tract infection, emotional upset or rarely, neurological problems.

In nocturnal enuresis, a careful history and examination are needed, but investigation other than urine dipstick testing is rarely necessary. The child with diurnal (daytime) enuresis, on the other hand, might need an ultrasound examination, including post-voiding to look for evidence of congenital anomalies and voiding dysfunction (‘irritable bladder’) (see Chapter 11, p. 125).

Children with enuresis are sometimes criticized and punished and have low self-esteem. It is important to emphasize that enuresis is involuntary, but that it normally resolves, and with some appropriate help, this might happen more quickly. In those children who develop secondary enuresis, consider the possibility of an organic cause, such as urinary tract infection, diabetes or a neurological disorder. Psychological distress (e.g. bereavement) may also manifest as secondary enuresis; however, in most children, enuresis (primary or secondary) is a benign variant of normal bladder control and is not associated with unhappiness or anxiety.