[Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome].

Abstract

Monitoring of blood glucose is usually reported to reduce the risk of hypoglycemia in term newborns with high risk factors and for prematurity in neonatal intensive care unit patients. Differential diagnosis has rarely been discussed. In the eutrophic term newborn, hypoglycemia remains rare and an etiological diagnosis must be made. Intensive management of neonatal hypoglycemia is required to prevent neurodevelopmental defects. Without evident cause or if hypoglycemia persists, a systematic review of possible causes should be made. We report isolated glucocorticoid deficiency diagnosed in an infant at 10 months of age. This boy had neonatal hypoglycemia and mild jaundice that had not been investigated. During his first 9 months of life, he presented frequent infections. At 10 months of age, febrile seizures occurred associated with shock, hypoglycemia, hyponatremia, mild hyperpigmentation, and coma. He was diagnosed with hypocortisolemia and elevated ACTH levels. Brain injury was revealed by MRI after resuscitation, with hypoxic-ischemic and hypoglycemic encephalopathy. The molecular studies demonstrated the presence of p.Asp107Asn and previously unreported frameshift p.Pro281GlnfsX9 MC2R gene mutations. A substitutive hormone therapy was provided and during a follow-up of 12 months no adrenal crisis was noted. We report an unusual case of familial glucocorticoid deficiency with severe neurological injury. This case demonstrates the importance of an appropriate etiological diagnosis in neonatal hypoglycemia.

• Authors: O Delmas, C Marrec, E Caietta, G Simonin, Y Morel, N Girard, F Roucher, J Sarles, B Chabrol, R Reynaud
• Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie (Arch Pediatr) Vol. 21 Issue 12 Pg. 1353-8 (Dec 2014) ISSN: 1769-664X [Electronic] France
• Vernacular Title: Hypoglycémie néonatale sévère et récidivante sans perte de sel révélatrice d'un syndrome de résistance à l'ACTH.
• PMID: 25445127 (Publication Type: Case Reports, English Abstract, Journal Article)
• Copyright: Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Topics

• Adrenal Insufficiency (complications)
• Humans
• Hypoglycemia (etiology)
• Infant, Newborn
• Male
• Steroid Metabolism, Inborn Errors (complications)