Literature DB >> 20081435

Developmental milestones in infants and young Australasian children with achondroplasia.

Penelope Jane Ireland1, Sarah Johnson, Samantha Donaghey, Leanne Johnston, James McGill, Andreas Zankl, Robert S Ware, Verity Pacey, Jenny Ault, Ravi Savarirayan, David Sillence, Elizabeth Thompson, Sharron Townshend.   

Abstract

BACKGROUND: Achondroplasia, the most common form of chondrodysplasia (inherited skeletal dysplasia), is characterized by a significant delay in the development of communication and motor skills, particularly during the first 2 years. Although some information regarding timing of development for children with achondroplasia is available, no study has evaluated simultaneously the pattern of skill development across multiple key developmental areas.
METHOD: This study used a retrospective questionnaire to quantify developmental data on milestone achievement. Twenty families of children with achondroplasia throughout Australia and New Zealand were asked to document age of acquisition for 41 gross motor, fine motor, and communication and feeding milestones. More than one half of the items assessed were milestones identified in the Australian State Government Personal Health Record Books. The results are compared with previously available information regarding development of motor skills by a cohort of American children with achondroplasia.
RESULTS: Although the results support previously reported delays in gross motor and communication skill development, fine motor development does not seem to be as delayed as previously suggested. Information on development of self-feeding skills is presented for the first time and occurs later in this group than the typically developing population. We describe 2 distinctive and previously unreported methods of transitioning between static positions commonly used by children with achondroplasia.
CONCLUSION: Delays were reported across gross motor and communication and feeding skills but were not observed during development of fine motor skills. Additional information is also offered regarding a variety of unusual movement strategies demonstrated by young children with achondroplasia.

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Year:  2010        PMID: 20081435     DOI: 10.1097/DBP.0b013e3181c72052

Source DB:  PubMed          Journal:  J Dev Behav Pediatr        ISSN: 0196-206X            Impact factor:   2.225


  13 in total

Review 1.  Systematic Review: Non-Instrumental Swallowing and Feeding Assessments in Pediatrics.

Authors:  Dani-Ella Heckathorn; Renée Speyer; Jessica Taylor; Reinie Cordier
Journal:  Dysphagia       Date:  2015-11-25       Impact factor: 3.438

2.  A registry of achondroplasia: a 6-year experience from the Czechia and Slovak Republic.

Authors:  Martin Pesl; Hana Verescakova; Linda Skutkova; Jana Strenkova; Pavel Krejci
Journal:  Orphanet J Rare Dis       Date:  2022-06-16       Impact factor: 4.303

Review 3.  Achondroplasia: a comprehensive clinical review.

Authors:  Richard M Pauli
Journal:  Orphanet J Rare Dis       Date:  2019-01-03       Impact factor: 4.123

4.  Natural history of 39 patients with Achondroplasia.

Authors:  Jose Ricardo Magliocco Ceroni; Diogo Cordeiro de Queiroz Soares; Larissa de Cássia Testai; Rachel Sayuri Honjo Kawahira; Guilherme Lopes Yamamoto; Sofia Mizuho Miura Sugayama; Luiz Antonio Nunes de Oliveira; Debora Romeo Bertola; Chong Ae Kim
Journal:  Clinics (Sao Paulo)       Date:  2018-07-02       Impact factor: 2.365

5.  Clinical Practice Guidelines for Achondroplasia.

Authors:  Takuo Kubota; Masanori Adachi; Taichi Kitaoka; Kosei Hasegawa; Yasuhisa Ohata; Makoto Fujiwara; Toshimi Michigami; Hiroshi Mochizuki; Keiichi Ozono
Journal:  Clin Pediatr Endocrinol       Date:  2020-01-09

6.  Development of the Screening Tool for Everyday Mobility and Symptoms (STEMS) for skeletal dysplasia.

Authors:  Penelope J Ireland; Ravi Savarirayan; Tash Pocovi; Tracy Tate; Marie Coussens; Louise Tofts; Craig Munns; Verity Pacey
Journal:  Orphanet J Rare Dis       Date:  2021-01-21       Impact factor: 4.123

Review 7.  Optimal management of complications associated with achondroplasia.

Authors:  Penny J Ireland; Verity Pacey; Andreas Zankl; Priya Edwards; Leanne M Johnston; Ravi Savarirayan
Journal:  Appl Clin Genet       Date:  2014-06-24

8.  Birth prevalence of achondroplasia: A systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Femke van Kessel; Rosa van Hoorn; Judith van den Bosch; Renée Shediac; Sarah Landis
Journal:  Am J Med Genet A       Date:  2020-08-17       Impact factor: 2.802

9.  Assessing physical symptoms, daily functioning, and well-being in children with achondroplasia.

Authors:  Kathryn M Pfeiffer; Meryl Brod; Alden Smith; Jill Gianettoni; Dorthe Viuff; Sho Ota; R Will Charlton
Journal:  Am J Med Genet A       Date:  2020-10-20       Impact factor: 2.802

10.  Assessing the impacts of having a child with achondroplasia on parent well-being.

Authors:  Kathryn M Pfeiffer; Meryl Brod; Alden Smith; Jill Gianettoni; Dorthe Viuff; Sho Ota; R Will Charlton
Journal:  Qual Life Res       Date:  2020-08-16       Impact factor: 4.147

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