A neonatal case of apolipoprotein C-II deficiency

descriptionPublicationkeyboard_double_arrow_right Article 01 Apr 1989 English Publisher:Springer Science and Business Media LLCJournal:European Journal of Pediatrics, volume 148, pages 550-552 (issn: 0340-6199, eissn: 1432-1076,

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Authors: M, Ohno; S, Ishibashi; K, Nakao; T, Nozue; K, Nonomura; N, Yamada; H, Aburatani; +2 Authors

doi: 10.1007/bf00441556

pmid: 2501098

A neonatal case of apolipoprotein C-II deficiency

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Abstract

A neonatal case of apo C-II deficiency with hypertriglyceridaemia and xanthomas is presented. The patient responded well to a special diet formula containing medium-chain triglycerides (MCT). This is the first case of apo C-II deficiency to be discovered during the neonatal period.

Related Organizations

Tachikawa Hospital
Japan
University of Tokyo
Japan

Keywords

Hypertriglyceridemia, Male, Genetic Diseases, Inborn, Infant, Newborn, Humans, Apolipoproteins C, Xanthogranuloma, Juvenile, Triglycerides

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