Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome

Introduction: Congenital hypopituitarism (CH) is characterized by a deficiency of one or more pituitary hormones. The pituitary gland is a central regulator of growth, metabolism, and reproduction. The anterior pituitary produces and secretes growth hormone (GH), adrenocorticotropic hormone, thyroid...

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Detalles Bibliográficos
Autores principales: Bosch i Ara, Laura, Katugampola, Harshini, Dattani, Mehul T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902025/
https://www.ncbi.nlm.nih.gov/pubmed/33634051
http://dx.doi.org/10.3389/fped.2020.600962

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902025/
https://www.ncbi.nlm.nih.gov/pubmed/33634051
http://dx.doi.org/10.3389/fped.2020.600962

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