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 Universite de Paris UW Libraries SJSU King Library SJSU King Library NUS Library McGill DET KGL BIBLiOTEK JCU Discovery Universidad De Lima WorldCat VU on WorldCat
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