Encephalopathy in type I hyperlipidemia.

Abstract:

:Familial chylomicronemia syndrome is a group of rare genetic disorders characterized by deficient activity of an enzyme lipoprotein lipase or apo-protein C-II deficiency. In this paper we present an infant with massive hyperchylomicronemia and severe pancreatitis. Exchange transfusion for controlling hypertriglyceridemia and pancreatitis led to an increase in hyperviscosity which resulted in encephalopathy.

journal_name

Indian Pediatr

journal_title

Indian pediatrics

authors

Onal H,Atugluzeybek C,Alhaj S,Altun G

subject

Has Abstract

pub_date

2007-04-01 00:00:00

pages

306-8

issue

4

eissn

0019-6061

issn

0974-7559

journal_volume

44

pub_type

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