Abstract
Carnitine palmitoyltransferase 1A (CPT1A) deficiency is a type of fatty acid oxidation
disorder in which long chain fatty acids cannot be transported into mitochondria for
further processing and storage in our body. Typically, the patients present with lethargy,
hypoglycemia, and raised serum transaminase levels before 2 years of age. Cholestatic
jaundice as manifestation of this deficiency has been reported rarely; here, we report
an adolescent male with CPT1A deficiency who developed prolonged cholestatic jaundice
following a febrile illness.
Keywords
cholestatic jaundice - CPT1A - clinical