Management of Neonatal Isolated and Combined Growth Hormone Deficiency: Current Status.
cognition disorders/physiopathology
congenital hypopituitarism
growth hormone
growth hormone deficiency
hormone replacement therapy
hypoglycaemia
newborn
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
14 Jun 2023
14 Jun 2023
Historique:
received:
08
05
2023
revised:
11
06
2023
accepted:
12
06
2023
medline:
29
6
2023
pubmed:
28
6
2023
entrez:
28
6
2023
Statut:
epublish
Résumé
Congenital growth hormone deficiency (GHD) is a rare disease caused by disorders affecting the morphogenesis and function of the pituitary gland. It is sometimes found in isolation but is more frequently associated with multiple pituitary hormone deficiency. In some cases, GHD may have a genetic basis. The many clinical signs and symptoms include hypoglycaemia, neonatal cholestasis and micropenis. Diagnosis should be made by laboratory analyses of the growth hormone and other pituitary hormones, rather than by cranial imaging with magnetic resonance imaging. When diagnosis is confirmed, hormone replacement should be initiated. Early GH replacement therapy leads to more positive outcomes, including reduced hypoglycaemia, growth recovery, metabolic asset, and neurodevelopmental improvements.
Identifiants
pubmed: 37373261
pii: ijms241210114
doi: 10.3390/ijms241210114
pmc: PMC10299208
pii:
doi:
Substances chimiques
Human Growth Hormone
12629-01-5
Pituitary Hormones
0
Growth Hormone
9002-72-6
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
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