Concurrent mutations of germline GPR101 and somatic USP8 in a pediatric giant pituitary ACTH adenoma: a case report

BACKGROUND: Cushing’s disease (CD) is rare in pediatric patients. It is characterized by elevated plasma adrenocorticotropic hormone (ACTH) from pituitary adenomas, with damage to multiple systems and development. In recent years, genetic studies have shed light on the etiology and several mutations...

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Detalles Bibliográficos
Autores principales: Bao, Xu-dong, Lu, Lin, Zhu, Hui-juan, Yao, Yong, Feng, Ming, Wang, Ren-zhi, Zhai, Xiao, Fu, Yong, Gong, Feng-ying, Lu, Zhao-lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169391/
https://www.ncbi.nlm.nih.gov/pubmed/35668434
http://dx.doi.org/10.1186/s12902-022-01058-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169391/
https://www.ncbi.nlm.nih.gov/pubmed/35668434
http://dx.doi.org/10.1186/s12902-022-01058-8

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