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Arm Span and Its Relation to Height in a 2- to 17-Year-Old Reference Population and Heterozygous Carriers of ACAN Variants
Department of Paediatrics, Maastricht University Medical Centre, Maastricht, The Netherlands.
Division of Paediatric Endocrinology and Centre for Molecular Medicine, Karolinska Institutet and University Hospital, Stockholm, Sweden.
Division of Endocrinology, Children's National Hospital, Washington, District of Columbia, USA; Department of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA.
Örebro University, School of Medical Sciences. Division of Paediatric Endocrinology and Centre for Molecular Medicine, Karolinska Institutet and University Hospital, Stockholm, Sweden; Department of Paediatrics, School of Medical Sciences, University Hospital, Örebro, Sweden.ORCID iD: 0000-0002-9986-8138
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2020 (English)In: Hormone Research in Paediatrics, ISSN 1663-2818, E-ISSN 1663-2826, Vol. 93, no 3, p. 164-172Article in journal (Refereed) Published
Abstract [en]

BACKGROUND/OBJECTIVES: In the clinical assessment of a short or tall child, estimating body disproportion is useful to assess the likelihood of a primary growth disorder, e.g., skeletal dysplasia. Our objectives were (1) to use data from the Maastricht study on healthy children (2-17 years) to calculate relative arm span (AS) for height (H) to serve as age references for clinical purposes; (2) to assess its age and sex dependency; and (3) to investigate relative AS adjustment for age and sex in individuals with ACAN haploinsufficiency.

METHODS: The Maastricht study data (2,595 Caucasian children, 52% boys, 48% girls) were re-analysed to produce reference tables and graphs for age and sex of AS - H and AS/H. Published information on AS/H in Europeans was used as reference data for adults. Relative AS from 33 patients with ACAN haploinsufficiency were plotted against reference data and expressed as standard deviation score (SDS) for age and sex.

RESULTS: Mean AS - H from 2 to 17 years increased from -1.2 to +1.5 cm in boys and from -4.8 to +1.6 cm in girls. Mean AS/H increased from 0.9848 to 1.0155 in boys and from 0.9468 to 1.0028 in girls. Mean AS/H in patients with ACAN haploinsufficiency was approximately 1.0, 1.5 and 0.5 SDS in young children, adolescents and 20- to 50-year-olds, respectively, and normal thereafter.

CONCLUSIONS: These reference charts can be used for 2- to 17-year-old children/adolescents. Carriers of ACAN haploinsufficiency have an elevated mean AS/H in childhood and adolescence and a slightly elevated ratio till 50 years.

Place, publisher, year, edition, pages
S. Karger, 2020. Vol. 93, no 3, p. 164-172
Keywords [en]
ACAN, Anthropometry, Arm span, Body proportions, Growth
National Category
Pediatrics
Identifiers
URN: urn:nbn:se:oru:diva-84236DOI: 10.1159/000508500ISI: 000570204500004PubMedID: 32575104Scopus ID: 2-s2.0-85087502675OAI: oai:DiVA.org:oru-84236DiVA, id: diva2:1460885
Funder
Swedish Research Council, K2015-54X-22 736-01-4 2015-02227VinnovaMarianne and Marcus Wallenberg FoundationStockholm County CouncilThe Karolinska Institutet's Research FoundationSwedish Society of Medicine
Note

Funding Agencies:

United States Department of Health & Human Services

National Institutes of Health (NIH) - USA

NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD) 1K23HD073351

IngaBritt och Arne Lundbergs forskningsstiftelse  

Byggmästare Olle Engkvist Stiftelse 

Erik och Edith Fernstrom Foundation for Medical Research  

Nyckelfonden  

Stiftelsen Frimurare Barnhuset i Stockholm 

Örebro University, Örebro, Sweden

Available from: 2020-08-25 Created: 2020-08-25 Last updated: 2020-10-02Bibliographically approved

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