The pharmacological management of obesity in Prader-Willi syndrome: what does the future hold?
Abstract
1. Prader-Willi syndrome (PWS) is a complex multisystem disorder, resulting from the lack of expression of paternally inherited imprinted genes on chromosome 15 (15q11.2-13). Three main genetic mec...
Fields of Study & Subjects
Genetic Syndromes and Imprinting
Hedgehog Signaling Pathway Studies
Apelin-related biomedical research
Publication details
- Journal / source
- Expert Opinion on Pharmacotherapy
- Publisher
- Informa UK Limited
- Volume
- 27
- Issue
- 5
- Pages
- 389–392
- Publication date
- 24 March 2026
- Language
- EN