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What is the Prader–Willi syndrome? – Part 3

• Prader–Willi syndrome is a rare genetic disorder. • In this syndrome seven genes (or some subset thereof) on chromosome 15 (q 11–13) are deleted or unexpressed (chromosome 15q partial deletion) on the paternal chromosome.

Diagnosis of Prader–Willi Syndrome

• Prader-Willi syndrome phenotype at 15 years of age. • Note the presence of typical PWS […]

What is the Prader–Willi syndrome? – Part 2

• Prader–Willi syndrome is a rare genetic disorder. • In this syndrome seven genes (or some subset thereof) on chromosome 15 (q 11–13) are deleted or unexpressed (chromosome 15q partial deletion) on the paternal chromosome.

Neuro-cognitive Symptoms

• Individuals with PWS are at risk of learning and attention difficulties. • Curfs and Fryns (1992) conducted […]