Results 41 to 50 of about 16,131 (205)

Changes in the spino-pelvic balance after hip replacement in patients with congenital hip dislocation

Хирургия позвоночника, 2018
Objective. To analyze the features of the sagittal spino-pelvic balance formation in patients with congenital hip dislocation and its changes after total hip replacement with restoration of the rotation center. Material and Methods.
Lev S. Shnaider, Vitaly V. Pavlov, Aleksandr V. Krutko, Vyacheslav A. Bazlov, Tariel Z. Mamuladze, Aleksey V. Peleganchuk   +5 more
doaj  

Congenital dislocation of the knee complicated with bilateral hip dislocation: a case report and literature review

BMC Musculoskeletal Disorders
Background Congenital dislocation of the knee is characterised by excessive knee extension or dislocation and anterior subluxation of the proximal tibia, and this disease can occur independently or coexist with different systemic syndromes. Nevertheless,
Bohai Qi, Qiang Jie, Xiaowei Wang, Qingda Lu, Fei Su, Yating Yang   +5 more
doaj   +1 more source

Dynamic ultrasonography in the diagnose of congenita/ dis/ocation of the hip (is dynamic ultrasonography necessary?)

Acta Orthopaedica et Traumatologica Turcica, 2020
A work has carried out our 100 hip series comprised 50 babies to evaluate benefits of dynamic methods besides the Graf method one of the ultrasonographic methods that is continuously widespread on the diagnose of congenital dislocation of the hip ...
Ali Okur, Fevzi Nakşılar, Bülent Alpaslan   +2 more
doaj  

Total hip arthroplasty in the treatment of neglected congenital dislocation or dysplasia of the hip

Acta Orthopaedica et Traumatologica Turcica, 2021
Objectives: We evaluated our methods and short-term results of total hip arthroplasty in the treatment of neglected congenital dislocation or dysplasia of the hip.\nMethods: We performed total hip arthroplasty in 13 hips of 11 female patients (mean age ...
Senol Akman, Cengiz Sen, Nadir Sener, I. Remzi Tozun   +3 more
doaj  

Recurrent spontaneous hip dislocation in a patient with neurofibromatosis type 1: a case report

Journal of Medical Case Reports, 2011
Introduction Neurofibromatosis type-1 is a common genetic disorder which often affects the skeleton. Skeletal manifestations of neurofibromatosis type-1 include scoliosis, congenital pseudarthrosis of the tibia and intraosseous cystic lesions ...
Harty James A, Butler Joseph S, Galbraith John G   +2 more
doaj   +1 more source

Expanding Phenotype of GINS1 Deficiency: A Case Report and Review of the Literature

Clinical Genetics, EarlyView.
The authors present a novel case and review of individuals with GINS1 deficiency, causing severe growth restriction and combined immunodeficiency. Only the ninth case of this ultrarare disorder, it highlights the role of these variants in disease, glaucoma as a feature, and the possibility of immunodeficiency without infections in affected individuals.
Michael P. Mackley, Rae Brager, Hannah Geddie, Vicky Breakey, Rebecca Hough, Dimitrios J. Stavropoulos, Vanda McNiven   +6 more
wiley   +1 more source

clinical homogeneity and allelic heterogeneity in seven patients [PDF]

, 2016
Background Larsen syndrome is an autosomal dominant skeletal dysplasia characterized by large joint dislocations and craniofacial dysmorphism. It is caused by missense or small in-frame deletions in the FLNB gene.
Bidchol, Abdul Mueed, Girisha, Katta Mohan, Graul-Neumann, Luitgard, Gupta, Ashish, Hehr, Ute, Kutsche, Kerstin, Lessel, Davor, Nader, Sean, Shah, Hitesh, Wickert, Julia   +9 more
core   +1 more source

Factors Influencing Sport‐Induced Bleeding in Patients With Haemophilia Without Inhibitors: A Single Centre Retrospective Study of People Born in the 2000s

Haemophilia, EarlyView.
ABSTRACT Introduction Recent advances in prophylaxis with clotting factor concentrates have enabled people with haemophilia (PwH) to participate in high‐intensity exercises; however, this does not preclude them from sports‐induced bleeding (SIB). Aim To investigate factors influencing the recent occurrence of SIB among PwH.
Rie Shirayama, Takuma Ito, Tetsuji Sato, Takayuki Hoshina   +3 more
wiley   +1 more source

Open Reduction and Internal Fixation of a Proximal Femoral Shaft Fracture in a Patient with Bilateral Congenital Hip Disease

Case Reports in Orthopedics, 2018
We present a rare case of a femoral shaft fracture in a 74-year-old woman with a preexisting untreated bilateral congenital hip dislocation and with concomitant leg length discrepancy.
Stefania Kanata, Antonios Anastasiadis
doaj   +1 more source

Anesthesia for a patient with Fanconi anemia for developmental dislocation of the hip: a case report

Brazilian Journal of Anesthesiology, 2014
Fanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with congenital and hematological abnormalities. Literature regarding the anesthetic management in these patients is limited.
Zafer Dogan, Huseyin Yildiz, Ismail Coskuner, Murat Uzel, Mesut Garipardic   +4 more
doaj   +1 more source