Cargando…
A Pilot Study Evaluating Therapeutic Response of Different Dosage of Oral Glucocorticoid in Two Children with Familial Glucocorticoid Deficiency Presenting with Diffuse Mucocutaneous Hyperpigmentation
INTRODUCTION: Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive potentially life-threatening condition, characterized by glucocorticoid deficiency, preserved aldosterone/renin secretion, and secondary rise in plasma adrenocorticotropic hormone level. This occurs due to either mu...
Autores principales: | Sarkar, Uttam Kumar, Sarma, Nilendu, Debbarma, Sambreeta, Mandal, Asok Kumar, Bala, Ashok Kumar |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363144/ https://www.ncbi.nlm.nih.gov/pubmed/28400640 http://dx.doi.org/10.4103/ijd.IJD_716_16 |
Ejemplares similares
-
Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in adolescence. Report of three siblings
por: Shivaprasad, K. S., et al.
Publicado: (2012) -
Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in an Egyptian child: a case report
por: Metwalley, Kotb A, et al.
Publicado: (2012) -
Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report
por: Uyangoda, Kanchana, et al.
Publicado: (2019) -
Mucocutaneous Findings in Hematolymphoid Neoplasms: An Observational Study
por: Batra, Anmol, et al.
Publicado: (2023) -
GDF15 Is Elevated in Conditions of Glucocorticoid Deficiency and Is Modulated by Glucocorticoid Replacement
por: Melvin, Audrey, et al.
Publicado: (2019)