Back to search

Article

Orthopedic manifestations in children with Prader-Willi syndrome

2023-12-12

Abstract excerpt

<h4>Background: </h4> Prader-Willi syndrome (PWS) is a rare genetic disease often associated with bone problems, mainly scoliosis and hip dysplasia (HD). This study aimed to analyze the clinical characteristics of orthopedic deformities in patients with PWS. Methods A retrospective study was conducted on 175 patients up to March 2023. The Cobb angle(CA) of the spine, the alpha angle of the hip joint, and the acet...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
e3fa1cc4-8e58-526e-b12d-5729af142571
DOI
10.21203/rs.3.rs-3715451/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Orthopedic manifestations in children with Prader-Willi syndromeDOI 10.21203/rs.3.rs-3715451/v1
The prevalence and surgical outcome of Hip Dysplasia in children with Prader-Willi SyndromeSemantic proximity
The musculoskeletal manifestations of Prader-Willi syndrome.Semantic proximity
Health Problems in Adults with Prader–Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the LiteratureSemantic proximity
High Prevalence of Hip Dysplasia in Patients with Scoliosis: A Retrospective StudySemantic proximity
A Review of the Principles of Radiological Assessment of Skeletal DysplasiasSemantic proximity
Bone health in children with Angelman Syndrome at the ENCORE Expertise CenterSemantic proximity
Clinical features, genetic detection and therapeutic response to rhGH of children with Noonan syndrome: an analysis of 12 cases.Semantic proximity
The Clinical and Genotypic Spectrum of Scoliosis in Multiple Pterygium Syndrome: A Case Series on 12 Children.Semantic proximity
Skeletal Survey of a Filipino Teenage Female with Ohdo syndrome: Case ReportSemantic proximity
Bone health in children with Angelman syndrome at the ENCORE Expertise Center.Semantic proximity
Musculo-skeletal phenotype of Costello syndrome and cardio-facio-cutaneous syndrome: insights on the functional assessment statusSemantic proximity
Achondroplasia and hypochondroplasia in France: a nationwide epidemiological analysisSemantic proximity
Select a neighboring publication to make it the new centre.