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A novel case of compound heterozygous congenital hyperinsulinism without high insulin levels
BACKGROUND: Congenital hyperinsulinism leads to unregulated insulin secretion and hypoglycemia. Diagnosis can be difficult and genetic testing may be warranted. CASE: This patient initially presented at 11 months with seizure activity secondary to severe hypoglycemia. Her diagnostic evaluation inclu...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502541/ https://www.ncbi.nlm.nih.gov/pubmed/26180531 http://dx.doi.org/10.1186/s13633-015-0012-4 |