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Growth & development 3
Ismail A-A Hassan (Ph. D., MRCPCH)
Developmental assessment
 Includes the quantification of delay in
relation to the child's chronological age.
 The main aim of developmental assessment
is early detection of delayed or abnormal
development
 This helps children achieve their maximum
chance of health and learning. This also
helps early start of treatment.
Developmental assessment
The sequence of developmental
milestones is the same.
It is the rate of acquiring
developmental skill that varies.
Developmental assessment
 Concentrate on each field of development
separately.
 Determine the stage the child reached for
each field.
 Relate the child developmental
achievement to the child chronological age.
 Relate the progress in each field to the
progress achieved in other fields.
Concentrate
Causes of developmental delay
 Predisposing factors:
 Congenital brain malformation
 Birth asphyxia
 CNS infections (meningitis & encephalitis)
 hypothyroidism
Causes of delayed motor
development:
 Familial
 Environmental factors: emotional
deprivation, lack of opportunity to
practice and malnutrition (rickets)
 Hypotonia (e. g. Down's syndrome)
Causes of delayed motor
development:
 Hypertonia (e. g. cerebral palsy)
 Neuromuscular disorders (as
Duchenne muscular dystrophy)
 Blindness
Causes of delayed speech or abnormal
language development:
 Familial
 Hearing impairment
 Environmental factors: emotional
deprivation and paucity of spoken
language at home.
Causes of delayed speech or
abnormal language development:
 Mental subnormality
 Autism
 Twins
 Cerebral palsy
 Dysphasia
Causes of visual impairment:
 Optic atrophy
 Congenital cataract
 Chorido-retinal degeneration
 Reterolental fibroplasia (retinopathy
of prematurity)
Causes of delayed sphincter control:
 Familial
 Mental subnormality
 Environmental factors: mismanagement of
toilet training
 Physical causes: meningomyelocele,
urterocele, ectopic ureter and posterior
uretheral valve
Hypothyroidism before treatment
The same child after treatment
How to determine the cause of
developmental delay:
 History:
 Seek family history
 A perinatal and postnatal history may
indicate a brain damaging event.
Examination:
 Full systemic examination
 Full neurological examination
 Look for dysmorphic appearance,
head circumference, neurocutaneous
features and spasticity or Hypotonia
Investigations:
 Thyroid function
 Serum calcium
 TORCH serology Chromosomal studies
 Blood creatin kinase (CK)
 Urine amino acids and organic acids
 Screen for mucopolysaccharides and blood
lactate.
Management of children with
severe developmental delay:
 Multidisciplinary team.
 A sympathetic and sensitive
explanation should be given to the
parents.
Management of children with
severe developmental delay:
 Physiotherapy: promoting full range of
movements to prevent deformities.
 Developmental stimulation: guidance in
stimulation and ways of encouraging the
development
 Genetic counseling: information
concerning the chance of recurrence of the
condition in their future children.
Education provision:
 Mild to moderate cases should be
encouraged to attend school with
normal children.
 Only severely handicapped children
should attend special schools for
children with special needs.
Prognosis of children with
developmental delay:
 Depends on the severity of the condition.
 Mild to moderate cases are capable of
leading independent near normal life.
 Children with severe developmental delay
remain dependents throughout life.
 The aim of education of such children is to
teach them self care ability.
Growth & development.ppt

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Growth & development.ppt

  • 1. Growth & development 3 Ismail A-A Hassan (Ph. D., MRCPCH)
  • 2. Developmental assessment  Includes the quantification of delay in relation to the child's chronological age.  The main aim of developmental assessment is early detection of delayed or abnormal development  This helps children achieve their maximum chance of health and learning. This also helps early start of treatment.
  • 3. Developmental assessment The sequence of developmental milestones is the same. It is the rate of acquiring developmental skill that varies.
  • 4. Developmental assessment  Concentrate on each field of development separately.  Determine the stage the child reached for each field.  Relate the child developmental achievement to the child chronological age.  Relate the progress in each field to the progress achieved in other fields.
  • 6. Causes of developmental delay  Predisposing factors:  Congenital brain malformation  Birth asphyxia  CNS infections (meningitis & encephalitis)  hypothyroidism
  • 7. Causes of delayed motor development:  Familial  Environmental factors: emotional deprivation, lack of opportunity to practice and malnutrition (rickets)  Hypotonia (e. g. Down's syndrome)
  • 8. Causes of delayed motor development:  Hypertonia (e. g. cerebral palsy)  Neuromuscular disorders (as Duchenne muscular dystrophy)  Blindness
  • 9. Causes of delayed speech or abnormal language development:  Familial  Hearing impairment  Environmental factors: emotional deprivation and paucity of spoken language at home.
  • 10. Causes of delayed speech or abnormal language development:  Mental subnormality  Autism  Twins  Cerebral palsy  Dysphasia
  • 11. Causes of visual impairment:  Optic atrophy  Congenital cataract  Chorido-retinal degeneration  Reterolental fibroplasia (retinopathy of prematurity)
  • 12. Causes of delayed sphincter control:  Familial  Mental subnormality  Environmental factors: mismanagement of toilet training  Physical causes: meningomyelocele, urterocele, ectopic ureter and posterior uretheral valve
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  • 17. The same child after treatment
  • 18. How to determine the cause of developmental delay:  History:  Seek family history  A perinatal and postnatal history may indicate a brain damaging event.
  • 19. Examination:  Full systemic examination  Full neurological examination  Look for dysmorphic appearance, head circumference, neurocutaneous features and spasticity or Hypotonia
  • 20. Investigations:  Thyroid function  Serum calcium  TORCH serology Chromosomal studies  Blood creatin kinase (CK)  Urine amino acids and organic acids  Screen for mucopolysaccharides and blood lactate.
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  • 22. Management of children with severe developmental delay:  Multidisciplinary team.  A sympathetic and sensitive explanation should be given to the parents.
  • 23. Management of children with severe developmental delay:  Physiotherapy: promoting full range of movements to prevent deformities.  Developmental stimulation: guidance in stimulation and ways of encouraging the development  Genetic counseling: information concerning the chance of recurrence of the condition in their future children.
  • 24. Education provision:  Mild to moderate cases should be encouraged to attend school with normal children.  Only severely handicapped children should attend special schools for children with special needs.
  • 25. Prognosis of children with developmental delay:  Depends on the severity of the condition.  Mild to moderate cases are capable of leading independent near normal life.  Children with severe developmental delay remain dependents throughout life.  The aim of education of such children is to teach them self care ability.