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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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| Publicado no: | J Clin Endocrinol Metab |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Endocrine Society
2018
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| Assuntos: | |
| Acesso em linha: | 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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