Literature DB >> 10968241

Osteogenesis imperfecta: profiles of motor development as assessed by a postal questionnaire.

R H Engelbert1, C S Uiterwaal, V A Gulmans, H E Pruijs, P J Helders.   

Abstract

UNLABELLED: This study was performed to achieve more detailed information regarding the age and sequence in the development of motor milestones in the different types of osteogenesis imperfecta (OI). The parents of 98 patients with a diagnosis of OI were sent a questionnaire regarding the age at which patients achieved motor milestones. All patients were attending the outpatient clinic for children with OI at the Wilhelmina Children's Hospital. The motor milestones were classified into static motor milestones and dynamic motor milestones and all data were checked with health care records. The age of development of motor milestones was compared to reference values of the healthy population. The severity of the disease was classified according to Sillence based on clinical, genetic and radiological data. The age of intramedullary rodding of the first nail in the lower and upper extremity and the localisation was noted. A total of 76 parents responded to the 98 questionnaires (78%). In OI type I, a delay exists in achieving motor milestones, comparable to the 95th percentile of the normal population. In type III, the development of all motor milestones was significantly delayed compared to types I and IV with a discrepancy between static and dynamic milestones. In OI type IV, a retardation in motor development developed after the milestone 'sitting without support' was achieved. Motor development in types I and IV was not influenced by intramedullary rodding of the lower extremities, since rodding was rarely performed before the milestone 'unsupported standing' was achieved. In type III, the influence of intramedullary rodding on the age of achieving motor milestones remains questionable.
CONCLUSION: The severity of osteogenesis imperfecta has a large influence on the age and sequence in the development of motor milestones. No influence of intramedullary rodding of the lower extremities on motor development was found in osteogenesis imperfecta types I and IV, whereas the influence in type III remains questionable.

Entities:  

Mesh:

Year:  2000        PMID: 10968241     DOI: 10.1007/s004310000505

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  6 in total

1.  Fassier-Duval femoral rodding in children with osteogenesis imperfecta receiving bisphosphonates: functional outcomes at one year.

Authors:  Joanne Ruck; Noémi Dahan-Oliel; Kathleen Montpetit; Frank Rauch; François Fassier
Journal:  J Child Orthop       Date:  2011-05-08       Impact factor: 1.548

2.  Intravenous pamidronate treatment of infants with severe osteogenesis imperfecta.

Authors:  Eva Aström; Håkan Jorulf; Stefan Söderhäll
Journal:  Arch Dis Child       Date:  2006-11-17       Impact factor: 3.791

3.  Quality of life in children with osteogenesis imperfecta treated with oral bisphosphonates (Olpadronate): a 2-year randomized placebo-controlled trial.

Authors:  Dieke H J Kok; Ralph J B Sakkers; Arieke J Janse; Hans E H Pruijs; Ab J Verbout; Rene M Castelein; Raoul H H Engelbert
Journal:  Eur J Pediatr       Date:  2007-02-17       Impact factor: 3.183

Review 4.  WHOLE-BODY VIBRATION EXERCISE IMPROVES FUNCTIONAL PARAMETERS IN PATIENTS WITH OSTEOGENESIS IMPERFECTA: A SYSTEMATIC REVIEW WITH A SUITABLE APPROACH.

Authors:  Danubia C Sá-Caputo; Carla da F Dionello; Éric Heleno F F Frederico; Laisa L Paineiras-Domingos; Cintia Renata Sousa-Gonçalves; Danielle S Morel; Eloá Moreira-Marconi; Marianne Unger; Mario Bernardo-Filho
Journal:  Afr J Tradit Complement Altern Med       Date:  2017-03-01

5.  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

6.  Association between joint hypermobility, scoliosis, and cranial base anomalies in paediatric Osteogenesis imperfecta patients: a retrospective cross-sectional study.

Authors:  Heidi Arponen; Outi Mäkitie; Janna Waltimo-Sirén
Journal:  BMC Musculoskelet Disord       Date:  2014-12-13       Impact factor: 2.362

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.