KETOTIC HYPOGLYCEMIA | |
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OMIM = Online Mendelian Inheritance of Men | |
unknown Detail information to gene locus by the National Center for Biotechnology Information NCBI: |
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R82.4, E16.2 | |
Ketotic hypoglycaemia is a common form of hypoglycaemia in childhood, should only be diagnosed after exclusion of disorders of carbohydrate, fat metabolism, syndromes, drugs (e.g. Propranolol) ... Fatty acid oxidation defects, hyperinsulinism and adrenal insufficiency should always be excluded prior to organising controlled fasts [Sreekantam S et al. 2017]. | |
Laboratory findings | 3-Hydroxybutyric acid inc (urine) D-Glucose dec (serum) Ketone bodies (urine) normal/inc (blood) Ketone bodies (urine) inc (urine) |
Symptoms | hypoglycemia ketosis, ketoacidosis onset, childhood onset, infancy vomiting |