𝔖 Bobbio Scriptorium
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Characteristics of the eating disorder in Prader-Willi syndrome: implications for treatment

✍ Scribed by A. J. Holland; J. Treasure; P. Coskeran; J. Dallow

Book ID
114740443
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
442 KB
Volume
39
Category
Article
ISSN
0964-2633

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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