Syndrome de Prader-Willi. Guide ALD
- MeSH Terms
- Congenital; Hereditary; and Neonatal Diseases and Abnormalities (C16); Genetic Diseases; Inborn (C16.320); Abnormalities (C16.131); Neurological Disorders / Nervous System Diseases (C10); Neurologic Manifestations (C10.597); Nutritional and Metabolic Diseases (C18); Nutrition Disorders (C18.654)
- Publication Scope
- assessment
- management
- Countries of Application
- France
- Guideline Publication Status
- Published
- Languages
- French
- Authors
- HAS (FR)
- Publication Year
- 2012