| Literature DB >> 26557586 |
Sushma Malik1, Ashutosh Abhimanyu Paldiwal2, Charusheela Sujit Korday3, Shruti Sudhir Jadhav4.
Abstract
Carnitine palmitoyltransferase II (CPTII) deficiency is a rare disorder of mitochondrial fatty acid oxidation with autosomal recessive mode of inheritance. Three classic forms of CPT II deficiency have been described namely the lethal neonatal form, severe infantile hepatocardiomuscular form and the myopathic form. We present a three-day-old female child, admitted to us for lethargy, icterus, low sugars and convulsions. Persistent non ketotic hypoglycaemia, hyperammonemia, raised liver enzymes with hepatomegaly and cardiomyopathy led to the suspicion of fatty acid oxidation defect. Tandem mass spectrometry helped to clinch the diagnosis of CPT II Deficiency in the present case.Entities:
Keywords: CPT II gene; Fatty acid oxidation; Non ketotic hypoglycaemia; Tandem mass spectrometry
Year: 2015 PMID: 26557586 PMCID: PMC4625305 DOI: 10.7860/JCDR/2015/13600.6560
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X