Great Ormond Street Hospital for Children, London, UK.
UCL Great Ormond Street Institute of Child Health, London, UK.
Am J Med Genet A. 2024 Feb;194(2):243-252. doi: 10.1002/ajmg.a.63431. Epub 2023 Oct 9.
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.
软骨发育不全症(HCH)是一种罕见的骨骼发育不良疾病,导致轻度身材矮小。目前针对该人群的生长参考图表十分匮乏。本研究收集了人体测量学数据,旨在为确诊软骨发育不全症的儿童生成身高、体重和头围(HC)生长参考图表。本研究从 14 个欧洲专门的骨骼发育不良中心收集了混合的纵向人体测量学数据和遗传分析结果。使用位置、比例和形状的广义加性模型生成生长图表。共收集了 188 名(79 名女性)0-18 岁确诊软骨发育不全症儿童的身高(983 次)、体重(896 次)和 HC(389 次)测量值。在接受基因检测的 84 名儿童中,92%(77 名)发现 FGFR3 存在致病性变异。本研究使用这些数据生成了身高、体重和 HC 的生长参考值,绘制了 0-4 岁和 0-16 岁年龄的 7 个百分位值从第 2 到第 98 的图表。HCH 特异性生长图表对这些儿童的临床护理非常重要。它们有助于确定是否存在影响生长和发育的其他合并症,并为任何前瞻性干预研究和试验提供重要的基准。