GNAS mutation is an unusual cause of primary adrenal insufficiency: a case report

BACKGROUND: Primary adrenal insufficiency in children has non-specific and extensive clinical features, so the diagnosis of its etiology is complex and challenging. Although congenital adrenal hyperplasia is the most common cause, more and more other genetic causes have been identified. GNAS mutatio...

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Detalles Bibliográficos
Autores principales: Tong, Yajie, Yue, Dongmei, Xin, Ying, Zhang, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351131/
https://www.ncbi.nlm.nih.gov/pubmed/35927642
http://dx.doi.org/10.1186/s12887-022-03517-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351131/
https://www.ncbi.nlm.nih.gov/pubmed/35927642
http://dx.doi.org/10.1186/s12887-022-03517-6

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