Background: There is no satisfactory or curative therapy for many of the disabling genetic
disorders such as Ekman-Lobstein syndrome (osteogenesis imperfecta). However, it is …

Introduction: Joint hypermobility (JH) is the hallmark of many hereditary soft connective
tissue disorders, including Ehlers-Danlos syndromes and related disorders, disorders of the …

The present paper aims at discussing the current manufacturing processes of chest
orthoses, considering patients affected by Osteogenesis Imperfecta (OI) and a possible …

Создание и ведение регистров пациентов с редкими болезнями помогает определить
их распространенность, оценить качество оказания медицинской помощи …

The sclera is a dense poorly vascularized connective tissue structure composed of Types I,
III, IV, V, VI, and VIII collagen. The characteristic blue sclera is caused by thinness and …

Background: Osteogenesis imperfecta (OI) is a heritable disease characterized by bone
fragility and other extra skeletal manifestations. Most patients with OI have mutations in the …

(1) Background: The aim of the work is to identify some imaging parameters in osteogenesis
imperfecta to assist the dentist in the diagnosis, planning, and orthodontic treatment of …

Osteogenesis imperfecta (OI) is a rare genetic connective-tissue disorder with bone fragility.
To avoid iatrogenic fractures, healthcare providers have traditionally avoided using non …

Objetivo: Comparar o ângulo de fase de pacientes com osteogênese imperfeita atendidos
em um hospital universitário terciário com pacientes de um grupo controle de crianças …

Antecedentes y objetivo La osteogénesis imperfecta es una enfermedad rara cuya
característica principal es la presencia de fragilidad ósea. Además, estos pacientes …