In this Article

• What is Prader-Willi syndrome?
• What are the signs, symptoms, and physical features of Prader-Willi syndrome?
• How common is, and what causes Prader-Willi syndrome?
• Can Prader-Willi syndrome be inherited?
• Where can I find information about treatment for Prader-Willi syndrome?
• Where can I find additional information about Prader-Willi syndrome?
• What other names do people use for Prader-Willi syndrome?
• What if I still have specific questions about Prader-Willi syndrome?
• Where can I find general information about genetic conditions?
• What glossary definitions help with understanding Prader-Willi syndrome?
• Prader-Willi Syndrome Index

• Prader-Labhart-Willi syndrome
  
  
• PWS

• See How can I find a genetics professional in my area? in the Handbook.

• Ask the Genetic and Rare Diseases Information Center.

The Handbook provides basic information about genetics in clear language.

• What does it mean if a disorder seems to run in my family?
• What is a chromosome?
• Can changes in the number of chromosomes affect health and development?
• Are chromosomal disorders inherited?
• What are genomic imprinting and uniparental disomy?

These links provide additional genetics resources that may be useful.

• Genetics and health
  
  
• Resources for Patients and Families
  
  
• Resources for Health Professionals