Clinical and genetic features of childhood-onset congenital combined pituitary hormone deficiency: a retrospective, single-center cohort study
Considering the high proportion of neonatal presentations, identification of the early neonatal features of hypopituitarism to manage pituitary and extrapituitary phenotypes is critical. The genetic etiology of cCPHD warrants further exploration.
Authors
- Jung Min Ko (ORCID: https://orcid.org/0000-0002-0407-7828)
- Yoonha Lee (ORCID: https://orcid.org/0000-0002-4702-3977)
- Choong Ho Shin (ORCID: https://orcid.org/0000-0002-9813-1134)
- Yun Jeong Lee (ORCID: https://orcid.org/0000-0003-2847-2643)
- Young Ah Lee (ORCID: https://orcid.org/0000-0001-9179-1247)
Institutions
- Seoul National University (KR)
- Seoul National University Children's Hospital (KR)
- Hallym University Dongtan Sacred Heart Hospital (KR)
Publication Details
- Journal
- Annals of Pediatric Endocrinology & Metabolism
- Published
- 2024-12-30
- DOI
- https://doi.org/10.6065/apem.2448008.004
- Citations
- 3
- Primary Topic
- Growth Hormone and Insulin-like Growth Factors
- Type
- article
- Field-Weighted Citation Impact
- 1.07