20p11.23-p11.21 deletion in a child with hyperinsulinemic hypoglycemia and GH deficiency: A case report

Some neonatal hypoglycemias have genetic origins. For instance, mutation in forkhead box protein A2 (FOXA2), located on chromosome 20p11.21, has recently been reported to cause hyperinsulinemic hypoglycemia and hypopituitarism. Here, we report a case of hyperinsulinemic hypoglycemia and GH deficienc...

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Detalles Bibliográficos
Autores principales: Sugawara, Daisuke, Matsuura, Misa, Sato, Hiroaki, Ohashi, Hirofumi, Ichihashi, Ko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267556/
https://www.ncbi.nlm.nih.gov/pubmed/34285455
http://dx.doi.org/10.1297/cpe.30.133

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267556/
https://www.ncbi.nlm.nih.gov/pubmed/34285455
http://dx.doi.org/10.1297/cpe.30.133

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