ESPE Abstracts

ESPE Abstracts

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Previous issue | Volume 98 | ESPE2024

62nd Annual ESPE (ESPE 2024)

Liverpool, UK
16 Nov 2024 - 18 Nov 2024

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The 62nd ESPE Annual Meeting will now be taking place in Liverpool, UK.

Symposia

Challenges in the management of Prader Willi Syndrome

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hrp0098s10.1 | Challenges in the management of Prader Willi Syndrome | ESPE2024

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hrp0098s10.2 | Challenges in the management of Prader Willi Syndrome | ESPE2024

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hrp0098s10.3 | Challenges in the management of Prader Willi Syndrome | ESPE2024

Growth hormone treatment in adults with PWS

Höybye Charlotte

Prader-Willi syndrome (PWS) is a rare, neurodevelopmental, genetic disorder in adults characterized by muscular hypotonia, a different body composition with more body fat than muscle mass, hyperphagia, behavioral challenges and cognitive dysfunction. Endocrine deficiencies, including growth hormone (GH) deficiency, are common. In many countries GH is approved for treatment of children with genetically confirmed PWS, whereas treatment of adolescents and adults is only approved ...
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