Last update 08 May 2025

Familial chylomicronaemia syndrome

Basic Info

Synonyms
Familial Chylomicronemia Syndrome, Familial chylomicronaemia syndrome, Familial chylomicronemia syndrome
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Introduction
A rare genetic hyperlipidaemia characterised by excessive increase in plasma triglyceride levels due to the accumulation of chylomicrons. Clinical manifestations include recurrent episodes of severe acute pancreatitis, abdominal pain, nausea, fatigue, diarrhoea, constipation, hepatosplenomegaly, eruptive xanthomas and failure to thrive. Children may often be asymptomatic. The condition is not associated with severe atherosclerosis.

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