Hypogonadism in Prader–Willi syndrome from birth to adulthood: a 28-year experience in a single centre

BACKGROUND: Hypogonadism is a key feature of Prader–Willi syndrome (PWS) but clear strategies for hormone replacement are lacking. OBJECTIVE: To evaluate the gonadal status and outcome in patients attending a Scottish PWS clinic from 1991 to 2019. METHODS: In 93 (35F:56M) patients, median follow-up...

Descripción completa

Detalles Bibliográficos
Autores principales: Kherra, Sakina, Forsyth Paterson, Wendy, Cizmecioglu, Filiz Mine, Jones, Jeremy Huw, Kourime, Mariam, Elsedfy, Heba Hassan, Tawfik, Sameh, Kyriakou, Andreas, Shaikh, Mohamad Guftar, Donaldson, Malcolm David Cairns
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494419/
https://www.ncbi.nlm.nih.gov/pubmed/34382580
http://dx.doi.org/10.1530/EC-21-0277

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494419/
https://www.ncbi.nlm.nih.gov/pubmed/34382580
http://dx.doi.org/10.1530/EC-21-0277

Ejemplares similares