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 …

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 …

Osteogenesis imperfecta (OI), also known as “brittle bone disease,” is a genetic bone
disorder. OI bones experience frequent fractures. Surgical procedures are usually followed …

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 …

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 …

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 …

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 …

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 …

Introdução: A Osteogênese Imperfeita (OI) é uma doença genética rara caracterizada pela
fragilidade óssea, fraturas aos mínimos traumas e deformidades. Essas alterações podem …

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 …