Prader Willi Syndrome Resource Center - All Articles

Prader Willi Syndrome - All Articles

Prader-Willi syndrome is a rare genetic condition that starts in infancy and causes physical, mental, and behavioral issues. Key symptoms present from birth include low muscle tone - babies often feel floppy when held - distinct facial features, and poor sucking reflex. As the child ages, they develop insatiable food cravings because they never feel full, as well as intellectual challenges and behavioral issues. Treatment is available and requires a high level of care from a team of specialists.

ALL PRADER WILLI SYNDROME ARTICLES

Meet Our Experts In Prader Willi Syndrome
Everyday Health’s team of board-certified physicians and health professionals contribute to the creation and review of content, ensuring that the information is useful, up to date, and accurate.
EDITORIAL SOURCES
Everyday Health follows strict sourcing guidelines to ensure the accuracy of its content, outlined in our editorial policy. We use only trustworthy sources, including peer-reviewed studies, board-certified medical experts, patients with lived experience, and information from top institutions.
Resources
  1. Prader-Willi Syndrome. Mayo Clinic. November 14, 2024.