Abstract

BackgroundAchondroplasia is the most common genetic skeletal disorder causing disproportionate short stature/dwarfism. Common additional features include spinal stenosis, midface retrusion, macrocephaly and a generalized spondylometaphyseal dysplasia which manifest as spinal cord compression, sleep disordered breathing, delayed motor skill acquisition and genu varus with musculoskeletal pain. To better understand the interactions and health outcomes of these potential complications, we embarked on a multi-center, natural history study entitled CLARITY (achondroplasia natural history study). One of the CLARITY objectives was to develop growth curves (length/height, weight, head circumference, weight-for-height) and corresponding reference tables of mean and standard deviations at 1 month increments from birth through 18 years for clinical use and research for achondroplasia patients.MethodsAll available retrospective anthropometry data including length/height, weight and head circumference from achondroplasia patients were collected at 4 US skeletal dysplasia centers (Johns Hopkins University, AI DuPont Hospital for Children, McGovern Medical School University of Texas Health, University of Wisconsin School of Medicine and Public Health). Weight-for-age values beyond 3 SD above the mean were excluded from the weight-for-height and weight-for-age curves to create a stricter tool for weight assessment in this population.ResultsOver 37,000 length/height, weight and head circumference measures from 1374 patients with achondroplasia from birth through 75 years of age were compiled in a REDCap database. Stature and weight data from birth through 18 years of age and head circumference from birth through 5 years of age were utilized to construct new length/height-for-age, weight-for-age, head circumference-for-age and weight-for-height curves.ConclusionAchondroplasia-specific growth curves are essential for clinical care of growing infants and children with this condition. In an effort to provide prescriptive, rather than purely descriptive, references for weight in this population, extreme weight values were omitted from the weight-for-age and weight-for-height curves. This well-phenotyped cohort may be studied with other global achondroplasia populations (e.g. Europe, Argentina, Australia, Japan) to gain further insight into environmental or ethnic influences on growth.

Highlights

  • Achondroplasia is the most common genetic skeletal disorder causing disproportionate short stature/ dwarfism

  • Achondroplasia-specific growth curves are essential for clinical care of growing infants and children with this condition

  • This wellphenotyped cohort may be studied with other global achondroplasia populations (e.g. Europe, Argentina, Australia, Japan) to gain further insight into environmental or ethnic influences on growth

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Summary

Introduction

Achondroplasia is the most common genetic skeletal disorder causing disproportionate short stature/ dwarfism. Monitoring growth of populations with short stature skeletal dysplasias presents challenges, given that the condition is relatively rare and relevant normative growth curves had, until recently, been limited to handsmoothed curves derived from US data published in 1977 and 1978 [1, 2] Subsequent growth references have been produced from populations with achondroplasia in the US [3,4,5,6,7], Europe [8, 9], Australia [10, 11], Argentina [12,13,14], Egypt [15] and Japan [16]. Merker et al [8] derived curves for similar outcomes in a northern

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