Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management

Hyperinsulinaemic hypoglycaemia (HH) is due to the unregulated secretion of insulin from pancreatic β-cells. A rapid diagnosis and appropriate management of these patients is essential to prevent the potentially associated complications like epilepsy, cerebral palsy and neurological impairment. The...

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Veröffentlicht in:	Journal of inherited metabolic disease 2012-07, Vol.35 (4), p.589-601
Hauptverfasser:	Senniappan, Senthil, Shanti, Balasubramaniam, James, Chela, Hussain, Khalid
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Biochemistry Biological and medical sciences Congenital Hyperinsulinism - diagnosis Congenital Hyperinsulinism - genetics Congenital Hyperinsulinism - pathology Congenital Hyperinsulinism - therapy Human Genetics Humans Insulin - metabolism Insulin-Secreting Cells - metabolism Insulin-Secreting Cells - pathology Internal Medicine Medical genetics Medical sciences Medicine Medicine & Public Health Metabolic Diseases Multimodal Imaging - methods Pancreatectomy - methods Pediatrics Positron-Emission Tomography Review Tomography, X-Ray Computed
Online-Zugang:	Volltext
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