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Sathyabama Ramachandram
Consultant Developmental Paediatrician
Hospital Pulau Pinang
Child Development
• Child development is a dynamic process.
• Gross motor
• Fine motor
• Speech language, communication
• Social
• Cognitive
Developmental Examination: Birth to 1 Year
Gross Motor Milestones
• Delay/disordered development marker for
motor disorders
• Motor abilities have weak correlation with
cognitive development
• Loss of primitive reflex by 3 months
• Appearance of supportive reflex by 4 months
• Improving postural control & stability in
cephalo-caudal direction
Examination/Observation Gross Motor
Fine Motor
• Maturing grasp: apposition of tips of fingers
with tip of thumb, palmar (6/12) pincer (9-
10/12) , finger tips (12/12)
• Release with open hands/pressure (10-
11/12); controlled release: puts 1 cube on
top of another (13/12)
Development of Grasp: Cube
Developmental Examination: Birth to 1 Year
Fine Motor examination
• Reaching, grasping, exploration
• Hand to hand transfer of a block placed in
front infant sitting supported
• Use a small object to prompt
• Encourage release of a block/toy in the
hand or container
• Placing one brick on another, indicating
mature release.
Visual Behaviour, eye-hand coordination &
problem solving
• Progressive coordination of maturing vision
with head, body & fine motor movements can
be observed through manipulation & use of
cubes, crayon, formboards etc
• Categorisation
Sharma 2011
Developmental Examination: 1- 5 years
Gross Motor
• Arm & leg posture and coordination
• Imitate a model
(child is shown how to do it)
• Copy a model
(child is shown a completed model)
Developmental Examination: 1- 5 years
Speech, Language & Communication
• Expressive
• Receptive (Comprehension)
• Speech Sound & Fluency
• 50% intelligible speech by 2 years
• Fully intelligible by 4 years
• Pragmatics
• 2 ½ - 3years can take turns in conversation
• 4 years, can converse skillfully
Developmental Examination: 1- 5 years
Speech, Language & Communication
• History:
• Does your child respond to your smile,
His/her name
“No”
Simple commands?
• What sounds does your child make in
response to you?
• Meaningful words?
Developmental Examination: 1- 5 years
Speech, Language & Communication
Genetic tests
Molecular karyotyping
Specific tests: Fragile X (FMR1), Prader Willi or Angelman
syndrome
Array-based comparative genomic hybridisation (aCGH) as a
first-tier investigation - not readily available.
Refer to clinical geneticist when syndromic features are present.
Investigations
Metabolic & Biochemical
• Blood :
• Urea & electrolytes, Creatine Kinase, Thyroid Function
Test, Full Blood Count, Amino Acid, Acyl-carnitine Profile
• Urine:
• Organic Acid, Oligosaccharides, Creatine/GAA, Purine
and pyrimidine
MRI brain
• Higher yield when associated with microcephaly, non-
familial macrocephaly, rapid change in head
circumference, focal neurological signs or epilepsy.
EEG if history of seizures
Management
Multidisciplinary approach
• Occupational therapy
• Speech therapist (if indicated)
• School placement : mainstream/inclusive/ integrated
class
• Extra training at government/private/NGO
intervention centres.
• Registration as Child with Special Needs
• Management of comorbidities
Thank you