Orthopedic manifestations in children with Prader-Willi syndrome

Abstract Background 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...

Full description

Bibliographic Details
Main Authors: Miao Miao, Guo-Qiang Zhao, Qiong Zhou, Yun-Qi Chao, Chao-Chun Zou
Format: Article
Language:English
Published: BMC 2024-02-01
Series:BMC Pediatrics
Subjects:
Online Access:https://doi.org/10.1186/s12887-024-04603-7