Optimising Health-Related Quality of Life in Children With Osteogenesis Imperfecta
CL Hill, D Ford, J Baker - Calcified Tissue International, 2024 - Springer
Osteogenesis Imperfecta is a rare, hereditary bone condition with an incidence of 1/15,000–
20,000. Symptoms include bone fragility, long bone deformity, scoliosis, hypermobility …
20,000. Symptoms include bone fragility, long bone deformity, scoliosis, hypermobility …
Musculoskeletal System and Gait Characteristics in patients with Osteogenesis Imperfecta
K Graff, M Kalinowska, E Szczerbik… - Clinical …, 2024 - journals.sagepub.com
Objectives The aim of the study was to assess the muscoloskeletal system and
spatiotemporal gait parameters of patients in three types of osteogenesis imperfecta. Design …
spatiotemporal gait parameters of patients in three types of osteogenesis imperfecta. Design …
Physiological loading-induced interstitial fluid dynamics in osteon of osteogenesis imperfecta bone
Osteogenesis imperfecta (OI), also known as “brittle bone disease,” is a genetic bone
disorder. OI bones experience frequent fractures. Surgical procedures are usually followed …
disorder. OI bones experience frequent fractures. Surgical procedures are usually followed …
[HTML][HTML] The impact of foot orthoses on gait in children with Osteogenesis Imperfecta type I, III and IV–a cross-sectional study
JE Naili, E Åström, J Löwing, M Reimeringer… - BMC Musculoskeletal …, 2024 - Springer
For children with Osteogenesis Imperfecta (OI), a rare genetic bone disease, walking can be
difficult to carry out due to a combination of bone fragility and deformity, muscle weakness …
difficult to carry out due to a combination of bone fragility and deformity, muscle weakness …
[HTML][HTML] Gait characterization in rare bone diseases in a real-world environment-a comparative controlled study
S Fink, M Suppanz, J Oberzaucher, MA Castro… - Gait & Posture, 2024 - Elsevier
Background Rare bone diseases (RBD) cause physical and sensory disability that affects
quality of life. Mobility challenges are common for people with RBDs, and travelling to gait …
quality of life. Mobility challenges are common for people with RBDs, and travelling to gait …
[HTML][HTML] Functional independence of Taiwanese children with osteogenesis imperfecta
YM Syu, CL Lee, CK Chuang, HC Chiu… - Journal of Personalized …, 2022 - mdpi.com
Osteogenesis imperfecta (OI) is a group of rare genetic disorders that affect bone formation.
Patients with OI present mainly with increased bone fragility and bone deformities. Twenty …
Patients with OI present mainly with increased bone fragility and bone deformities. Twenty …
Consistent inconsistencies in braking: a spatial analysis
AG Hammerberg, PA Kramer - Interface Focus, 2021 - royalsocietypublishing.org
The dynamic system that is the bipedal body in motion is of interest to engineers, clinicians
and biological anthropologists alike. Spatial statistics is more familiar to public health …
and biological anthropologists alike. Spatial statistics is more familiar to public health …
Periodização e prescrição de treino na osteogênese imperfeita: revisão sistemática
JCS Guimarães, AV Costa, MFS Dias - Research, Society and …, 2023 - rsdjournal.org
Osteogenesis imperfecta (OI) is a congenital and chronic atavistic disease that affects bones
through their fragility, linked to the process of deterioration of bone connective tissue. The …
through their fragility, linked to the process of deterioration of bone connective tissue. The …
Avaliação da funcionalidade de crianças e adolescentes com osteogênese imperfeita
ACN Fernandes - 2021 - lume.ufrgs.br
Introdução: A Osteogênese Imperfeita (OI) é uma doença genética rara caracterizada pela
fragilidade óssea, fraturas aos mínimos traumas e deformidades. Essas alterações podem …
fragilidade óssea, fraturas aos mínimos traumas e deformidades. Essas alterações podem …
MOTOR DEVELOPMENT AND GAIT OF CHILDREN WITH OSTEOGENESIS IMPERFECTA: LITERATURE REVIEW
KG da Silva, KSVB Pereira… - Health and …, 2022 - periodicojs.com.br
For hereditary reasons, an individual can develop a deficit in the COL1A1 and COL1A2
genes, resulting in a lack of collagen and causing imperfect osteogenesis. Thus, this work …
genes, resulting in a lack of collagen and causing imperfect osteogenesis. Thus, this work …