Time for a general approval of growth hormone treatment in adults with Prader–Willi syndrome

Abstract Prader-Willi syndrome (PWS) is a complex, multi-system, neurodevelopmental disorder characterised by neonatal muscular hypotonia, short stature, high risk of obesity, hypogonadism, intellectual disabilities, distinct behavioural/psychiatric problems and abnormal body composition with increa...

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Bibliografiska uppgifter

Huvudupphov:	Charlotte Höybye, Anthony J. Holland, Daniel J. Driscoll, The Clinical and Scientific Advisory Board of The International Prader-Willi Syndrome Organisation
Materialtyp:	Artigo
Språk:	Inglês
Utgiven:	BMC 2021-02-01
Serie:	Orphanet Journal of Rare Diseases
Ämnen:	Prader-willi syndrome Growth hormone Growth hormone treatment Adults
Länkar:	https://doi.org/10.1186/s13023-020-01651-x
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