Growth reference charts for children with hypochondroplasia

Moira S. Cheung*, Tim J. Cole, Paul Arundel, Nicola Bridges, Christine P. Burren, Trevor Cole, Justin Huw Davies, Lars Hagenäs, Wolfgang Högler, Anthony Hulse, Avril Mason, Ciara McDonnell, Andrea Merker, Klaus Mohnike, Ataf Sabir, Mars Skae, Anya Rothenbuhler, Justin Warner, Melita Irving

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Hypochondroplasia (HCH) is a rare skeletal dysplasia causing mild short stature. There is a paucity of growth reference charts for this population. Anthropometric data were collected to generate height, weight, and head circumference (HC) growth reference charts for children with a diagnosis of HCH. Mixed longitudinal anthropometric data and genetic analysis results were collected from 14 European specialized skeletal dysplasia centers. Growth charts were generated using Generalized Additive Models for Location, Scale, and Shape. Measurements for height (983), weight (896), and HC (389) were collected from 188 (79 female) children with a diagnosis of HCH aged 0–18 years. Of the 84 children who underwent genetic testing, a pathogenic variant in FGFR3 was identified in 92% (77). The data were used to generate growth references for height, weight, and HC, plotted as charts with seven centiles from 2nd to 98th, for ages 0–4 and 0–16 years. HCH‐specific growth charts are important in the clinical care of these children. They help to identify if other comorbidities are present that affect growth and development and serve as an important benchmark for any prospective interventional research studies and trials.
Original languageEnglish
Number of pages10
JournalAmerican Journal of Medical Genetics Part A
Early online date9 Oct 2023
DOIs
Publication statusE-pub ahead of print - 9 Oct 2023

Keywords

  • hypochondroplasia
  • head circumference
  • weight
  • height
  • anthropometry
  • growth

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