Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Short femoral neck"'
Publikováno v:
Christiansen, J D, Ejaz, A, Nielsen, P T & Laursen, M 2020, ' An Ultra-Short Femoral Neck-Preserving Hip Prosthesis : A 2-Year Follow-up Study with Radiostereometric Analysis and Dual X-Ray Absorptiometry in a Stepwise Introduction ', Journal of Bone and Joint Surgery: American Volume, vol. 102, no. 2, pp. 128-136 . https://doi.org/10.2106/JBJS.19.00104
BACKGROUND: Total hip arthroplasty (THA) with a diaphyseal stem may risk bone loss. In order to save proximal bone stock in young patients with a high activity level and a long life expectancy, the interest in short stems has evolved. The purpose of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab86bb80d806c126d1529ed9eedd51f3
https://vbn.aau.dk/da/publications/155de8e5-de39-4b0d-a888-b860459ff4de
https://vbn.aau.dk/da/publications/155de8e5-de39-4b0d-a888-b860459ff4de
Autor:
Christopher M. Larson, Ira Zaltz
Publikováno v:
The Journal of Hip Surgery. :126-134
Although femoroacetabular impingement (FAI) is traditionally considered an intra-articular phenomenon, the result of abutment between the femoral head and/or neck and the acetabular rim, there are unique and relatively uncommon patterns of pathologic
Publikováno v:
Clinical Orthopaedics & Related Research. 476:1479-1490
Background When treatment of acute septic arthritis of the hip is delayed, severe sequelae can occur. This may take the form of coxa breva, vara, or valga. Pseudoarthrosis of the femoral neck is a rare complication with only a few studies to guide tr
Publikováno v:
European Journal of Medical Genetics. 64:104343
Acrocapitofemoral dysplasia (ACFD) is a rare autosomal recessive skeletal dysplasia characterized by short stature with short limb dwarfism, brachydactyly, and a narrow thorax. Major radiographic features are egg-shaped capital femoral epiphyses with
Publikováno v:
Journal of pediatric orthopedics. 39(4)
Background Femoral neck lengthening and transfer of the greater trochanter were introduced by Morscher as treatment for patients with coxa breva and overgrowth of the greater trochanter. In this study we evaluated intermediate and long-term results o
Autor:
Waleed Mekki, Mikhail Teplenky
Publikováno v:
Journal of Children's Orthopaedics
Purpose Proximal femoral ischemic deformities in the pediatric population is a challenging pathological situation. Many surgical techniques have been proposed to treat this problem, with variable reported results. We believe that a C-shaped pertrocha
Publikováno v:
Clinical Pediatric Endocrinology. 25:103-106
Gain-of-function mutations in the fibroblast growth factor receptor 3 gene (FGFR3) result in a group of skeletal dysplasias, such as prototypic achondroplasia (ACH: OMIM #100800) and lethal thanatophoric dysplasia (TD1: OMIM #187600). Hypochondroplas
Autor:
Michael D. Ries
Publikováno v:
Journal of Bone and Joint Surgery. 102:e9
Autor:
Perry L. Schoenecker, John C. Clohisy
Publikováno v:
Pediatric Pelvic and Proximal Femoral Osteotomies ISBN: 9783319780320
Following the occurrence and healing of Legg-Calve-Perthes (LCP) in childhood, residual hip joint deformity of variable severity can occur, which is characterized by morphological features of both femoral acetabular impingement (FAI) and variable sec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7275b179dfe9e03bdd2a50036d7fed5a
https://doi.org/10.1007/978-3-319-78033-7_37
https://doi.org/10.1007/978-3-319-78033-7_37
Publikováno v:
Journal of Orthopaedic Surgery, Vol 24 (2016)
PurposeTo review the outcome of Wagner double intertrochanteric osteotomy for trochanteric overgrowth and a short femoral neck in 7 adolescents.MethodsRecords of one male and 6 females aged 15 to 20 years who underwent modified Wagner osteotomy for t