Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report

BACKGROUND: Familial glucocorticoid deficiency is a rare autosomal recessive disorder characterized by isolated glucocorticoid deficiency. Most patients are diagnosed following episodes of hypoglycemia or convulsion. We report the case of an infant with familial glucocorticoid deficiency who present...

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Detalles Bibliográficos
Autores principales: Uyangoda, Kanchana, Kamalanathan, Phirarthana, Mettananda, Sachith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6724328/
https://www.ncbi.nlm.nih.gov/pubmed/31481085
http://dx.doi.org/10.1186/s13256-019-2206-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6724328/
https://www.ncbi.nlm.nih.gov/pubmed/31481085
http://dx.doi.org/10.1186/s13256-019-2206-5

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