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Seizure frequency and characteristics in children with Down syndrome

✍ Scribed by Hadassa Goldberg-Stern; Richard H. Strawsburg; Bonnie Patterson; Fran Hickey; Mary Bare; Natan Gadoth; Ton J. Degrauw

Book ID
117545455
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
97 KB
Volume
23
Category
Article
ISSN
0387-7604

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Prader-Willi syndrome (PWS) is a genomic imprinting disorder, which is due to the loss of a functional paternal copy of 15q11-q13. Four different genetic mechanisms can lead to PWS: a paternal deletion of the 15q11-q13 region, maternal uniparental disomy (UPD), a defect in the imprinting center, or