A dual etiology of neonatal hypoglycemia secondary to FOXA2 heterozygous deletion
The role of the FOXA2 gene in both conditions highlights the need for awareness and precise diagnosis to ensure timely and appropriate treatment. This case underscores the complexity of neonatal hypoglycemia, where dual endocrine pathologies can coexist, necessitating comprehensive and careful evaluation.
Authors
- Marc Nicolino (ORCID: https://orcid.org/0000-0001-5395-2249)
- Kévin Perge (ORCID: https://orcid.org/0000-0002-6527-805X)
- Matthias Stamm
- Carine Villanueva (ORCID: https://orcid.org/0000-0003-3945-0431)
- Sara Cabet (ORCID: https://orcid.org/0000-0003-0115-2586)
- Lucie Bazus
Institutions
- Université Claude Bernard Lyon 1 (FR)
- Hôpital Femme Mère Enfant (FR)
- Centre Hospitalier Universitaire de Saint-Étienne (FR)
Publication Details
- Journal
- Hormone Research in Paediatrics
- Published
- 2025-05-26
- DOI
- https://doi.org/10.1159/000546342
- Primary Topic
- Hyperglycemia and glycemic control in critically ill and hospitalized patients
- Type
- article
- Field-Weighted Citation Impact
- 0.00