Lennox-gastaut syndrome in a pediatric patient with prader-willi syndrome: A case report and review

Prader-Willi Syndrome is typically caused by paternal deletion of chromosome 15q11-q13. It involves multiple systems and is commonly associated with hypotonia, global developmental delay, and endocrine abnormalities. Seizures are less frequently reported in individuals with Prader-Willi syndrome. He...

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Bibliographic Details

Published in:	Brain Disorders
Main Authors:	Raidah Albaradie, Sharook Alhawaj, Wojod Alothman, Shahid Bashir
Format:	Article
Language:	English
Published:	Elsevier 2025-03-01
Subjects:	Prader-Willi Syndrome seizure drop attacks Lennox-Gastaut Syndrome
Online Access:	http://www.sciencedirect.com/science/article/pii/S2666459325000216