Osteogenesis imperfecta (OI) is the most prevalent heritable bone fragility disorder in
children. It has been known for three decades that the majority of individuals with OI have …

Background Osteogenesis imperfecta (OI) is a rare heritable connective tissue disorder
primarily characterised by skeletal deformity and fragility, and an array of secondary …

Background: This review paper aims to report on the last 5 years of relevant research on
pediatric bone health in regard to nutrition and obesity, ethnic disparities, common …

Vitamin D affects several body functions, and thus general health, due to its pleiotropic
activity. It plays a key role in bone metabolism, and its deficiency impacts bone development …

Objective Studies on the baseline vitamin D levels in osteogenesis imperfecta (OI) patients
before medication are scarce. This study assessed the vitamin D status of a population with …

Osteogenesis Imperfecta (OI) is a heterogeneous group of inherited skeletal dysplasias
characterized by bone fragility. The study of bone metabolism, in these disease, is …

Purpose Skeletal dysplasia are heterogeneous conditions affecting the skeleton. Common
nutrition issues include feeding difficulties, obesity, and metabolic complications. This …

Backround Osteogenesis imperfecta (OI) is a frequent bone fragility disorder in children. The
purpose of this study was to assess the BMD and Vitamin D level in children with OI in …

Despite having different aetiologies, different rare bone diseases (RBDs) such as
hypophosphatasia (HPP), autosomal dominant hypophosphatemic rickets (ADHR), X-linked …

Background In several bone disorders, adequate calcium intake is a coadjuvant intervention
to regular treatment. Osteogenesis imperfecta (OI) is a collagen disorder with a range of …