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  • Title: [Prader-Willi syndrome in 22-year-old man--case study].
    Author: Kardas P, Adamiak-Kardas M.
    Journal: Wiad Lek; 2001; 54(11-12):709-14. PubMed ID: 11928560.
    Abstract:
    Prader-Willi syndrome is a rare genetic disorder with characteristic neonatal hypotonia, followed by obesity, low height, hypogonadism and mental retardation. In this paper a case of 22-year-old man suffering from Prader-Willi syndrome is described.
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