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Growth reference charts for children with hypochondroplasia.
Cheung, Moira S; Cole, Tim J; Arundel, Paul; Bridges, Nicola; Burren, Christine P; Cole, Trevor; Davies, Justin Huw; Hagenäs, Lars; Högler, Wolfgang; Hulse, Anthony; Mason, Avril; McDonnell, Ciara; Merker, Andrea; Mohnike, Klaus; Sabir, Ataf; Skae, Mars; Rothenbuhler, Anya; Warner, Justin; Irving, Melita.
Afiliação
  • Cheung MS; Great Ormond Street Hospital for Children, London, UK.
  • Cole TJ; UCL Great Ormond Street Institute of Child Health, London, UK.
  • Arundel P; Sheffield Children's Hospital NHS Foundation Trust, Sheffield, UK.
  • Bridges N; Department of Paediatric Endocrinology, Chelsea and Westminster Hospital, London, UK.
  • Burren CP; Paediatric Endocrinology and Diabetes Department, Bristol Royal Hospital for Children, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, UK.
  • Cole T; Birmingham Health Partners, West Midlands Regional Genetics Service, Birmingham Women's and Children's National Health Service (NHS) Foundation Trust, Birmingham, UK.
  • Davies JH; Regional Centre for Paediatric Endocrinology, University Hospital Southampton NHS Foundation Trust, Southampton Children's Hospital, University of Southampton, Southampton, UK.
  • Hagenäs L; Paediatric Endocrine Unit, Paediatric Clinic, Karolinska Hospital, Stockholm, Sweden.
  • Högler W; Institute of Metabolism & Systems Research, University of Birmingham, Birmingham, UK.
  • Hulse A; Evelina Children's Hospital, St. Thomas' Hospital, London, UK.
  • Mason A; Department of Endocrinology (E.M.F.), Queen Elizabeth University Hospital, Glasgow, UK.
  • McDonnell C; Department of Paediatric Endocrinology & Diabetes, Children's Health Ireland, Dublin, Ireland.
  • Merker A; Discipline of Paediatrics, School of Medicine, Trinity College Dublin, Dublin, Ireland.
  • Mohnike K; Department of Women and Child Health, Karolinska Institute, Stockholm, Sweden.
  • Sabir A; Department of Paediatrics, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
  • Skae M; Birmingham Health Partners, West Midlands Regional Genetics Service, Birmingham Women's and Children's National Health Service (NHS) Foundation Trust, Birmingham, UK.
  • Rothenbuhler A; Department of Pediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK.
  • Warner J; Department of Endocrinology and Diabetology for Children, Bicetre Paris-Saclay University Hospital, Le Kremlin Bicetre, France.
  • Irving M; Noah's Ark Children's Hospital for Wales, University Hospital of Wales, Cardiff, UK.
Am J Med Genet A ; 194(2): 243-252, 2024 Feb.
Article em En | MEDLINE | ID: mdl-37814549
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias / Osso e Ossos / Deformidades Congênitas dos Membros / Nanismo / Lordose Limite: Child / Female / Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias / Osso e Ossos / Deformidades Congênitas dos Membros / Nanismo / Lordose Limite: Child / Female / Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido