References

  1. Naville D, Penhoat A, Bégeot M. Syndromes de résistance à l'ACTH. Ann Endocrinol (Paris). 2000 Nov; 61(5):428-39.

  2. Delmas O, Marrec C, Caietta E, Simonin G et al. Hypoglycémie néonatale sévère et récidivante sans perte de sel révélatrice d'un syndrome de résistance à l'ACTH. Arch Pediatr. 2014 Dec; 21(12):1353-8. Google Scholar

  3. Menon S, Kuhn JM. Insuffisance surrénalienne. EMC Endocrinologie-Nutrition. 2011; 10: 015-A-10.

  4. Cooray SN, Chan L, Metherell L, Storr H et al. Adrenocorticotropin resistance syndromes. Endocr Dev. 2008; 13:99-116. PubMed | Google Scholar

  5. Chan LF, Clark AJ, Metherell LA. Familial glucocorticoid deficiency: advances in the molecular understanding of ACTH action. Horm Res. 2008; 69(2):75-82. PubMed | Google Scholar

  6. Chung TT, Chan LF, Metherell LA, Clark AJ. Phenotypic characteristics of familial glucocorticoid deficiency type 1 and 2. Clin Endocrinol (Oxf). 2010 May; 72(5): 589-594. PubMed | Google Scholar

  7. Kershnar AK, Roe TF, Kogut MD. Adrenocorticotropic hormone unresponsiveness: report of a girl with excessive growth and review of 16 reported cases. J Pediatr. 1972 Apr; 80(4):610-9. PubMed | Google Scholar

  8. Migeon CJ, Kenny FM, Kowarski A et al. The syndrome of congenital adrenocortical unresponsiveness to ACTH: report of six cases. Pediatr Res. 1968 Nov; 2 (6):501-13. PubMed | Google Scholar

  9. Thistlethwaite D, Darling JAB, Fraser R, Mason PA et al. Familial glucocorticoid deficiency. Study of diagnosis and pathogenesis. Arch Dis Child. 1975 Apr;50(4):291-7. Google Scholar

 

 

 

 

 

 

 

 

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