Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism

Congenital hyperinsulinism (CHI), a major cause of persistent and recurrent hypoglycemia in infancy and childhood. Numerous pathogenic genes have been associated with 14 known genetic subtypes of CHI. Adenosine triphosphate-sensitive potassium channel hyperinsulinism (KATP-HI) is the most common and...

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Detalles Bibliográficos
Autores principales: Zhang, Wei, Sang, Yan-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567654/
https://www.ncbi.nlm.nih.gov/pubmed/34736508
http://dx.doi.org/10.1186/s13023-021-02088-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567654/
https://www.ncbi.nlm.nih.gov/pubmed/34736508
http://dx.doi.org/10.1186/s13023-021-02088-6

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