Heterozygous Insulin Receptor (INSR) Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series

Mutations in the insulin receptor (INSR) gene are associated with insulin resistance and hyperglycaemia. Various autosomal dominant heterozygous INSR mutations leading to hyperinsulinemic hypoglycaemia (HH) have been described in adults and children (more than 3 years of age) but not in the neonatal...

Descripción completa

Detalles Bibliográficos
Autores principales: Sethi, Aashish, Foulds, Nicola, Ehtisham, Sarah, Ahmed, Syed Haris, Houghton, Jayne, Colclough, Kevin, Didi, Mohammed, Flanagan, Sarah E., Senniappan, Senthil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711633/
https://www.ncbi.nlm.nih.gov/pubmed/31989990
http://dx.doi.org/10.4274/jcrpe.galenos.2019.2019.0106

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711633/
https://www.ncbi.nlm.nih.gov/pubmed/31989990
http://dx.doi.org/10.4274/jcrpe.galenos.2019.2019.0106

Ejemplares similares