نتایج جستجو برای: anesthesia in osteogenesis imperfecta

تعداد نتایج: 16986453  

Journal: :International Journal of Pediatric Endocrinology 2015

Journal: :BMC Musculoskeletal Disorders 2020

Journal: :Ortopedia, traumatologia, rehabilitacja 2008
Elzbieta Jakubowska-Pietkiewicz Danuta Chlebna-Sokół

INTRODUCTION Osteogenesis imperfecta (OI) is a genetic disorder caused by a mutation in the genes that encode the chains of type I collagen. Clinical manifestations include increased bone fragility and blue sclerae. OI type III is the most severe form with fractures occurring already in utero. Fracture immobilisation and orthopaedic surgery are the mainstay of treatment for patients with OI, an...

2008
Thomas S Lisse Frank Thiele Helmut Fuchs Wolfgang Hans Gerhard K. H Przemeck Koichiro Abe Birgit Rathkolb Leticia Quintanilla-Martinez Gabriele Hoelzlwimmer Miep Helfrich Eckhard Wolf Stuart H Ralston Martin Hrabé de Angelis

Osteogenesis imperfecta is an inherited disorder characterized by increased bone fragility, fractures, and osteoporosis, and most cases are caused by mutations affecting the type I collagen genes. Here, we describe a new mouse model for Osteogenesis imperfecta termed Aga2 (abnormal gait 2) that was isolated from the Munich N-ethyl-N-nitrosourea mutagenesis program and exhibited phenotypic varia...

Journal: :Acta biochimica Polonica 2011
Agnieszka Rusińska Maria Świątkowska Wiktor Koziołkiewicz Szymon Skurzyński Joanna Golec Danuta Chlebna-Sokół

UNLABELLED The aim of the study is proteomic analysis of the plasma profile in children with recurrent bone fractures. The study involved 16 children: 6 patients with recurrent low-energy fractures and normal bone mass and 10 with osteogenesis imperfecta. In the analysis of the protein profile, the two-dimensional protein electrophoresis was used (Ettan DALT II, Amersham Bioscience). The images...

2016

Bowing of long bones may be secondary to several aetiologies. Among the causes for bowing of long bones include congenital and acquired form of rickets, skeletal dysplasia, osteogenesis imperfecta and renal tubular acidosis (RTA).

Journal: :The Journal of bone and joint surgery. British volume 1991
J Lammens A Mukherjee P Van Eygen G Fabry

A case of osteogenesis imperfecta, presenting with bowed deformity of both forearm bones and dislocation of the radial head was treated by separate elongation of both bones using Ilizarov's external fixator.

Journal: :Current opinion in pediatrics 2008
Paul Esposito Horacio Plotkin

PURPOSE OF REVIEW The treatment of osteogenesis imperfecta requires a multidisciplinary team to maximize function and comfort, and decrease fracture incidence. Medical treatment with bisphosphonates has allowed for safer, more effective surgical management of children with osteogenesis imperfecta. The purpose of this review is to outline treatment indications and choices of surgical techniques ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید