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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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Vydáno v:Clin Pediatr Endocrinol
Hlavní autoři: Sugawara, Daisuke, Matsuura, Misa, Sato, Hiroaki, Ohashi, Hirofumi, Ichihashi, Ko
Médium: Artigo
Jazyk:Inglês
Vydáno: The Japanese Society for Pediatric Endocrinology 2021
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8267556/
https://ncbi.nlm.nih.gov/pubmed/34285455
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.30.133
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