Prader-Willi Syndrome: Kyphoscoliosis is an underdiagnosed problem in young patients

    DOI Logo 10.17352/ijsr.000018

    Published On: February 09, 2021 | Pages: 001 - 003

    Author(s): Tahboub S*, Gross-Tsur V, Hirsch JH and Arzi H
    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 these children. Routine orthopedic examination for young children with PWS is e ... CrossMark Publons Harvard Library HOLLIS Search IT Semantic Scholar Get Citation Base Search Scilit OAI-PMH ResearchGate Academic Microsoft GrowKudos
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