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...

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Detalles Bibliográficos
Autores principales: Metwalley, Kotb A, Farghaly, Hekma S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
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

Internet

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

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