Oral Therapy in a Diabetic Patient With History of Infantile Hyperinsulinism

Abstract

Hyperinsulinism is the most common cause of persistent hypoglycemia in early infancy (1). Loss of function mutation in HNF4A gene is an unusual cause of this disease (2). HNF4A protein is a homodimer nuclear transcription factor with 474 amino acids which plays a role in 22 identified pathways. Mutations in this gene cause deficiency in regulation of beta… (More)
DOI: 10.5812/ijp.268

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