نتایج جستجو برای: congenital hip dysplasia

تعداد نتایج: 199119  

2014
Ernest L. Sink Benjamin F. Ricciardi Katrina Dela Torre Charles T. Price

PURPOSE One goal of neonatal screening for developmental dysplasia of the hip (DDH) is the prevention of late surgery. However, the majority of patients with acetabular dysplasia at skeletal maturity are not diagnosed with DDH during infancy. Selective ultrasound screening may identify patients with neonatal hip instability, but may be ineffective for the prevention of dysplasia presenting in a...

Journal: :The Journal of bone and joint surgery. British volume 1996
M Dickob T Martini

We implanted 300 uncoated cementless PM prostheses into 271 patients and followed 251 (92.6%) of them for four to seven years. By then 37 had already been revised for aseptic and three for septic loosening. The survival rate with implant failure as the endpoint was 88.8% for the cup and 85.3% for the stem after six years. There was a higher risk of implant loosening in congenital dysplasia, uni...

Journal: :The Journal of bone and joint surgery. British volume 1985
D A Sherlock P H Gibson M K Benson

In 1957 Somerville and Scott described their "direct approach" to the management of established congenital dislocation of the hip; arthrography after a period of traction served to distinguish the dislocated from the subluxated hip. We review the long-term outcome of hips which, using their criteria, were subluxated; 72 hips have been reviewed at periods ranging from 15 to 37 years after treatm...

Journal: :iranian journal of child neurology 0
zia islami md,fellowship of neonatology, associate professor, department of pediatrics, shahid sadoughi university of medical sciences, yazd, iran hosein ataii nakhaei resident, department of pediatrics, shahid sadoughi university of medical sciences, yazd, iran razieh fallah assistant professor of pediatric neurology, department of pediatrics, shahid sadoughi university of medical sciences, yazd, iran

camptomelic dysplasia (cmd) is a rare autosomal dominant congenital dwarfism characterized by shortness and bowing of long bones (camptomelia) and other severe skeletal and extra skeletal malformations. cmd is generally considered to be lethal and the majority of cases die in the neonatal period due to respiratory insufficiency. we hereunder report a term male neonate with characteristic clinic...

Journal: :Otolaryngology–Head and Neck Surgery 2010

Journal: :Archives of disease in childhood. Fetal and neonatal edition 2008
K Green S Oddie

This paper reviews the evidence regarding whether a standardised examination in the newborn period can improve infant health. The review considers aspects of delivering such a service from timing and number of examinations through to who should perform examinations, and whether evidence supports current practice. Infants at higher risk of anomaly such as those born preterm are highlighted. Aspe...

Journal: :European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie 2016
Michael Amir Kertai Wolfgang H Rösch Roland Brandl Horst Hirschfelder Nadine Zwink Anne Karoline Ebert

Introduction Abnormalities of the bony pelvis in exstrophy-epispadias complex (EEC) and their possible relation to hip disease are well described. However, there is a lack of information about long-term orthopedic consequences and hip function in patients with EEC. Therefore, we investigated clinical and radiological results in an EEC patient cohort after long-term follow-up. Patients and Metho...

Journal: :British Journal of Ophthalmology 1955

Abstract: Background: Ellis–Van-Creveld syndrome (EVC), otherwise known as chondroectodermal dysplasia. EVC presents several skeletal manifestations and congenital heart malformations. EVC syndrome consists of a tetrad of principal features: chondroectodermal dysplasia, polydactyly, congenital heart defects, and hypoplastic nails and teeth. In this syndrome alteration in the mechanical proper...

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