Neonatal hyperlipidemia with pancreatitis: Novel gene mutation of lipoprotein lipase

Lipoprotein lipase (LPL) deficiency is an autosomal recessive metabolic disorder with varying presentation in infancy and childhood, whereas clinical manifestations are rare in neonatal period. The estimated prevalence is one in a million births. A 23-day-old baby was admitted with complaints of fev...

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Bibliographic Details
Main Authors: M H Shah, R Roshan, R Desai, S S Kadam
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Journal of Postgraduate Medicine
Subjects:
Online Access:http://www.jpgmonline.com/article.asp?issn=0022-3859;year=2018;volume=64;issue=4;spage=247;epage=249;aulast=Shah