Results 31 to 40 of about 40,560 (235)

THE RESULTS OF TOTAL HIP JOINT ENDOPROSTHESIS FOR CONGENITAL HIP DISLOCATION

Паёми Сино, 2017
Objective: To study the results of total hip joint endoprosthesis for congenital hip dislocation. Methods: 62 patients (61 women and 1 man) with congenital hip dislocation performed hip joint endoprosthesis.
J.M. SAFAROV
doaj   +1 more source

Cri du Chat Syndrome and congenital dislocation of the hips and knees: case report. [PDF]

Rev Fac Cien Med Univ Nac Cordoba
Introduction: Cri Du Chat Syndrome (CdCS) is an autosomal genetic disorder involving the complete or partial deletion of the short arm of chromosome 5 (5p). The size of the CdCS deletion ranges from approximately 10-45 Mb.
Graça NNJ, Ribeiro MLA, Duarte ML.
europepmc   +2 more sources

Unilateral Congenital Knee and Hip Dislocation with Bilateral Clubfoot – A rare Packaging disorder

Journal of Orthopaedic Case Reports, 2013
ntroduction: Reduced intrauterine space gives rise to ‘packaging disorder’ which may involve joint dislocations or contractures. We present an unique case where mutiple joints were dislocated involving left congenital knee dislocation (CDK), bilateral ...
Mukesh Tiwari, Nishith Sharma
doaj   +1 more source

Total hip arthroplasty in patients with severe hip dysplasia and congenital pubic diastasis: report of two cases

BMC Musculoskeletal Disorders, 2021
Background Congenital bladder exstrophy is a rare malformation which is often associated with pubic diastasis and hip dysplasia. We reported the case two patients who underwent total hip arthroplasty (THA) due to advanced osteoarthritis combined with ...
Christian Goetze, Filippo Migliorini, Christian Dominik Peterlein   +2 more
doaj   +1 more source

APPLICATIONS OF KINETOTHERAPY IN CONGENITAL HIP DISLOCATION [PDF]

Annals of the “Ştefan cel Mare” University: Physical Education and Sport Section - The Science and Art of Movement, 2018
The congenital hip dislocation is one of the serious limb malformations, which untreated on time determines functional sequelae with high degree of disability.
Danelciuc Francisc Tadeus
doaj  

Congenital Hip Dislocation: A Rare Case in Adulthood

Acta Médica Portuguesa, 2018
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Natália Ferreira, Marcelo Abreu, Armando Abreu   +2 more
doaj   +1 more source

Shortening subtrochanteric osteotomy of the femur in total hip arthroplasty in patients with congenital hip dislocation

Гений oртопедии, 2020
Congenital hip dislocation in adults (Crowe type IV) is an indication for hip replacement. Shortening subtrochanteric osteotomy of the femur reduces the risk of vascular and neurological complications and corrects the antetorsion of the proximal femur ...
Lev S. Shnaider, Оleg I. Golenkov, E.U. Turgunov, Maksim V. Efimenko, M.A. Stepankova, Vitaliy V. Pavlov   +5 more
doaj   +1 more source

The Ilizarov technology for closed reduction of hip dislocation in children with developmental hip dysplasia

Гений oртопедии, 2021
Introduction The possibility of gradual closed reduction of hip dislocation in children over 1.5 years old is considered doubtful. Purpose Analysis of long-term results of applying the Ilizarov technique of gradual closed reduction in combination with ...
Mikhail P. Teplenky, Evgenii V. Oleinikov, Vyacheslav S. Bunov   +2 more
doaj   +1 more source

Prevalence of Developmental Dysplasia of the Hip in a Maternity Hospital in São Paulo, Brazil

Revista Brasileira de Ortopedia, 2021
Objective To evaluate the prevalence of developmental dysplasia of the hip (DDH), that is, hips classified as Graf type-IIc or higher, among a sample of the population of newborns aged from 0 to 3 days of life, and to correlate the findings with the main
Giovanna Galvão Braga Motta, Alessandra Rodrigues Silva Chiovatto, Eduardo Davino Chiovatto, Márcio Luís Duarte, Natasha Vogel Majewski Rodrigues, Wagner Iared   +5 more
doaj   +2 more sources

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