Prader-Willi Syndrome: Kyphoscoliosis is an underdiagnosed problem in young patients
<p>Prader-Willi Syndrome (PWS) is a complex, neurogenetic, multisystem disorder with a prevalence of 1:15000 to 1:30000, caused by lack of expression of genes in the paternally inherited chromosome 15q 11.2-q13. In this report we aim to characterize and increase awareness of kyphoscoliosis in...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
International Journal of Spine Research - Peertechz Publications,
2021-02-09.
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| Online Access: | Connect to this object online. |
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