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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Materias: | |
| 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 |