Prader-Willi Syndrome (PWS)

    Researchedby:
    Nick Milazzo
    Last Updated: October 13, 2024

    Prader Willi Syndrome is a genetic disorder that with symptoms that include muscle weakness, poor growth development, obesity, and a short stature.

    examine-databaseExamine Database

    Prader-Willi Syndrome (PWS) falls under the Other category.

    26 participants in 1 trial

    Examine Database: Prader-Willi Syndrome (PWS)

    Examine Database References

    1. Prader-Willi Syndrome Symptoms - Urs Eiholzer, Udo Meinhardt, Valentin Rousson, Nelica Petrovic, Michael Schlumpf, Dagmar l'AllemandDevelopmental profiles in young children with Prader-Labhart-Willi syndrome: effects of weight and therapy with growth hormone or coenzyme Q10Am J Med Genet A.(2008 Apr 1)