Prader–Willi syndrome: Symptoms and topiramate response in light of genetics

INTRODUCTION: Prader–Willi Syndrome (PWS) is a rare genetic condition, which affects one in 25,000 births and results in various phenotypes. It leads to a wide range of metabolic and endocrine disorders including growth delay, hypogonadism, narcolepsy, lack of satiety and compulsive eating, associat...

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Detalles Bibliográficos
Autores principales: Louveau, Cécile, Turtulici, Mimi-Caterina, Consoli, Angèle, Poitou, Christine, Coupaye, Muriel, Krebs, Marie-Odile, Chaumette, Boris, Iftimovici, Anton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939745/
https://www.ncbi.nlm.nih.gov/pubmed/36814790
http://dx.doi.org/10.3389/fnins.2023.1126970

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939745/
https://www.ncbi.nlm.nih.gov/pubmed/36814790
http://dx.doi.org/10.3389/fnins.2023.1126970

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