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...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2021-02-01
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Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13023-020-01651-x |