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Congenital hyperinsulinism presenting with different clinical, biochemical and molecular genetic spectra
Enver Şimşek1, Çiğdem Binay, Sarah E Flanagan
1Division of Pediatric Endocrinology, Department of Pediatrics University College London, London, United Kingdom. enversimsek06@hotmail.com.
Abstract:
Congenital hyperinsulinism (CHI) is a common cause of hypoglycemia in infants. We report three cases of CHI with differing clinical, biochemical, and molecular genetic spectra. One patient was unresponsive to medical treatment and died after subtotal pancreatectomy because of complications due to the surgery. Two patients have been followed successfully with medical treatment. Early diagnosis and appropriate treatment of CHI are essential to prevent morbidity and mortality.
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