A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature

Prader–Willi syndrome (PWS) is a rare genetic disorder resulting from lack of expression of the paternally derived chromosome 15q11–13, associated with several complications, including pubertal disorders, short stature, hyperphagia, obesity, glucose metabolism abnormalities, scoliosis, obstructive s...

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Detalles Bibliográficos
Autores principales: Aureli, Alessia, Bocchini, Sarah, Mariani, Michela, Crinò, Antonino, Cappa, Marco, Fintini, Danilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130376/
https://www.ncbi.nlm.nih.gov/pubmed/37124733
http://dx.doi.org/10.3389/fendo.2023.1148318

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130376/
https://www.ncbi.nlm.nih.gov/pubmed/37124733
http://dx.doi.org/10.3389/fendo.2023.1148318

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