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  • Title: Prader-Willi syndrome.
    Author: Couper R.
    Journal: J Paediatr Child Health; 1999 Aug; 35(4):331-4. PubMed ID: 10457284.
    Abstract:
    Prader-Willi syndrome is a multi system disorder characterized by neonatal hypotonia, later obesity, hyperphagia and mental retardation. It occurs sporadically, either as a result of microdeletion of chromosome 15p (70%) or as a result of maternal disomy of chromosome 15 (30%). The major problems encountered by parents are those of hyperphagia, food-seeking and obesity, and conduct disorder, particularly tantrums or oppositional behaviour.
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