Early diagnosis in familial glucocorticoid deficiency

Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive condition, characterized by marked atrophy of zona fasiculata and reticalaris with preservation of zona glomerulosa. Out of more than 50 published cases, 18 patients died as a result of glucocorticoid insufficiency. The main obje...

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Detalles Bibliográficos
Autores principales: Al Jneibi, Fatima, Hen, Tawfiq, Rajah, Jaishen, Nair, Rajendran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Research Paper/Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402699/
https://www.ncbi.nlm.nih.gov/pubmed/28458768
http://dx.doi.org/10.1080/19381980.2017.1310787

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402699/
https://www.ncbi.nlm.nih.gov/pubmed/28458768
http://dx.doi.org/10.1080/19381980.2017.1310787

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