Neonatal presentation of familial glucocorticoid deficiency with a MRAP mutation: A case report()

Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disorder in which the adrenal cortex fails to respond appropriately to stimulation by adrenocorticotropic hormone (ACTH) to produce cortisol. The disease is characterized in laboratory testing by glucocorticoid deficiency and mar...

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Detalles Bibliográficos
Autores principales: Chen, Chun, Zhou, Rui, Fang, Yanlan, Jiang, Liqiong, Liang, Li, Wang, Chunlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021926/
https://www.ncbi.nlm.nih.gov/pubmed/27660747
http://dx.doi.org/10.1016/j.ymgmr.2016.09.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021926/
https://www.ncbi.nlm.nih.gov/pubmed/27660747
http://dx.doi.org/10.1016/j.ymgmr.2016.09.003

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