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- W2245569439 abstract "Although Prader—Willi and Angelman syndromes are genetically related, they are as different as one might imagine in their associated behavioral and physical features. First identified 45 years ago, Prader—Willi syndrome (PWS) (1) is characterized by infantile hypotonia, hypogonadism, short stature, characteristic facial features, mild levels of cognitive delay, hyperphagia, increased risks of obesity, and obsessive—compulsive and other behavioral problems. Table 1 summarizes some of the associated facial and physical features of PWS, as agreed on by the consensus clinical diagnostic criteria for this syndrome (2). Of these, PWS is perhaps most famous for its characteristic hyperphagia and food-seeking behaviors. Indeed, even with today’ s improved early detection and intervention, complications of obesity remain the leading cause of death associated with this syndrome." @default.
- W2245569439 created "2016-06-24" @default.
- W2245569439 creator A5035397223 @default.
- W2245569439 creator A5073524560 @default.
- W2245569439 date "2003-01-01" @default.
- W2245569439 modified "2023-09-23" @default.
- W2245569439 title "Prader-Willi and Angelman Syndromes" @default.
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- W2245569439 doi "https://doi.org/10.1007/978-1-59259-353-8_6" @default.
- W2245569439 hasPublicationYear "2003" @default.
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