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

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

IntroductionPrader–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, associated...

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Bibliographic Details
Main Authors: Cécile Louveau, Mimi-Caterina Turtulici, Angèle Consoli, Christine Poitou, Muriel Coupaye, Marie-Odile Krebs, Boris Chaumette, Anton Iftimovici
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-02-01
Series:Frontiers in Neuroscience
Subjects:
Prader–Willi
topiramate
treatment
genetics
deletion
disomy
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2023.1126970/full

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https://www.frontiersin.org/articles/10.3389/fnins.2023.1126970/full

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