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

Prader-Willi Syndrome (PWS)

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•Last Updated: August 16, 2022

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

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

26 participants in 1 trial

Last Updated:August 16, 2022

26 participants in 1 trial

Examine Database: Prader-Willi Syndrome (PWS)

Intervention	Health Outcome	Grade	Evidence	Effect
Coenzyme Q10	1 Outcome		1 Study

1 Outcome

1 Study

1 Study

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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)