Neglected Chronically Dislocated Hip in a Prader-Willi Child: A Case Report and Literature Review
Introduction: Prader-Willi syndrome (PWS) is an uncommon genetic disorder resulting from the loss of function of genes in the paternal copy of chromosome 15q11.2-q13. Although the clinical features and diagnosis of PWS are well described, the management protocol for hip dysplasia (HD) is still contr...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Indian Orthopaedic Research Group
2025-03-01
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| Series: | Journal of Orthopaedic Case Reports |
| Subjects: | |
| Online Access: | https://jocr.co.in/wp/2025/03/01/neglected-chronically-dislocated-hip-in-a-prader-willi-child-a-case-report-and-literature-review/ |
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