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Congenital Hyperinsulinism and Hypopituitarism Attributable to a Mutation in FOXA2

CONTEXT: Persistent hypoglycemia in the newborn period most commonly occurs as a result of hyperinsulinism. The phenotype of hypoketotic hypoglycemia can also result from pituitary hormone deficiencies, including growth hormone and adrenocorticotropic hormone deficiency. Forkhead box A2 (Foxa2) is a...

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Bibliografiske detaljer
Udgivet i:J Clin Endocrinol Metab
Main Authors: Vajravelu, Mary Ellen, Chai, Jinghua, Krock, Bryan, Baker, Samuel, Langdon, David, Alter, Craig, De León, Diva D
Format: Artigo
Sprog:Inglês
Udgivet: Endocrine Society 2018
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6276717/
https://ncbi.nlm.nih.gov/pubmed/29329447
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2017-02157
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