Searchable abstracts of presentations at key conferences in endocrinology

ea0015p86 | Clinical practice/governance and case reports | SFEBES2008

Case report: hypoglycaemia, ketosis and lactic acidosis in a 17 year old: atypical presentation of an inborn error of metabolism

Kazmi Azra , Suresh Damodharan , Kim Soo-Hyun , Elvey Michael , Bouloux Pierre MG

Introduction: Fructose-1,6-bisphosphatase (FBPase) deficiency is an autosomal recessive disorder causing failure of gluconeogenesis. Multiple mutations may produce the disease, of which 960/961insG is the commonest and is pan-ethnic. Hypoglycaemia, ketosis and lactic acidosis associated with the condition are triggered by infection, fasting or fructose/sucrose/sorbitol intake.Aim: To present an atypical case of FBPase deficiency and to demonstrate findin...