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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2019
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| 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 |