Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in an Egyptian child: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/article/10.1186/1752-1947-6-110/fulltext.html
Reference12 articles.
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2. Shepard TH, Landing BH, Mason DG: Familial Addison's disease; case reports of two sisters with corticoid deficiency unassociated with hypoaldosteronism. AMA J Dis Child. 1959, 97: 154-162.
3. Thistlethwaite D, Darling JA, Fraser R, Mason PA, Rees LH, Harkness RA: Familial glucocorticoid deficiency. Studies of diagnosis and pathogenesis. Arch Dis Child. 1975, 50 (4): 291-297. 10.1136/adc.50.4.291.
4. Chung TT, Chan LF, Metherell LA, Clark AJ: Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2. Clin Endocrinol. 2010, 72: 589-594. 10.1111/j.1365-2265.2009.03663.x.
5. Metherell LA, Chapple JP, Cooray S, David A, Becker C, Rüschendorf F, Naville D, Begeot M, Khoo B, Nürnberg P, Huebner A, Cheetham ME, Clark AJ: Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2. Nat Genet. 2005, 37: 166-170. 10.1038/ng1501.
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