Literature DB >> 23430491

Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA Deficiency.

A A M Morris1, S E Olpin, M J Bennett, A Santani, J Stahlschmidt, P McClean.   

Abstract

Liver dysfunction usually accompanies metabolic decompensation in fatty acid oxidation disorders, including carnitine palmitoyltransferase (CPT) Ia deficiency. Typically, the liver is enlarged with raised plasma transaminase activities and steatosis on histological examination. In contrast, cholestatic jaundice is rare, having only been reported in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency. We report a 3-year-old boy with CPT Ia deficiency who developed hepatomegaly and cholestatic jaundice following a viral illness. No cause for the jaundice could be found, apart from the fatty acid oxidation disorder. Liver histology showed diffuse, predominately macrovesicular steatosis, hepatocellular and canalicular cholestasis but no bile duct paucity or evidence of large duct obstruction. The liver dysfunction resolved in 4-7 weeks.

Entities:  

Year:  2012        PMID: 23430491      PMCID: PMC3575043          DOI: 10.1007/8904_2012_135

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  9 in total

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6.  Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia.

Authors:  J A Ibdah; M J Dasouki; A W Strauss
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  9 in total
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2.  Carnitine palmitoyl transferase 1A deficiency in an adult with recurrent severe steato hepatitis aggravated by high pathologic or physiologic demands: A roller-coaster for internists.

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  2 in total

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