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Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in an Egyptian child: a case report
INTRODUCTION: Familial glucocorticoid deficiency, or hereditary unresponsiveness to adrenocorticotropic hormone, is a rare autosomal recessive disease characterized by glucocorticoid deficiency in the absence of mineralocorticoid deficiency. It may present in infancy or early childhood with hyperpig...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369203/ https://www.ncbi.nlm.nih.gov/pubmed/22507176 http://dx.doi.org/10.1186/1752-1947-6-110 |