Developmental milestones in infants and young Australasian children with achondroplasia

Penelope Jane Ireland1, Sarah Johnson, Samantha Donaghey

  • 1Queensland Paediatric Rehabilitation Service, Royal Children's Hospital, Brisbane, Queensland, Australia. penny_ireland@health.qld.gov.au

Insights

Children with achondroplasia experience delays in gross motor, communication, and feeding skills. However, fine motor development appears less impacted than previously thought, with unique movement strategies observed.

Area of Science:

  • Pediatrics
  • Genetics
  • Developmental Biology

Background:

  • Achondroplasia is the most common inherited skeletal dysplasia.
  • It is associated with significant delays in motor and communication skills in early childhood.
  • Previous studies have not comprehensively assessed skill development across multiple domains.

Purpose of the Study:

  • To quantify developmental milestone achievement in children with achondroplasia.
  • To compare skill development patterns across gross motor, fine motor, communication, and feeding domains.
  • To document novel movement strategies in young children with achondroplasia.

Main Methods:

  • Retrospective questionnaire distributed to 20 families in Australia and New Zealand.
  • Data collected on the age of acquisition for 41 developmental milestones.
  • Milestones included gross motor, fine motor, communication, and feeding skills, with many from the Australian Personal Health Record Books.

Main Results:

  • Gross motor and communication skills show expected delays.
  • Fine motor development is not as delayed as previously suggested.
  • Self-feeding skills emerge later than in typically developing children; novel transitional movement strategies are described.

Conclusions:

  • Developmental delays are confirmed in gross motor, communication, and feeding skills for children with achondroplasia.
  • Fine motor skill development does not appear significantly delayed.
  • Unusual movement strategies are common in young children with this condition.
Abstract

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