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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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Detaylı Bibliyografya
Yayımlandı:J Postgrad Med
Asıl Yazarlar: Shah, MH, Roshan, R, Desai, R, Kadam, SS
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6198689/
https://ncbi.nlm.nih.gov/pubmed/30147083
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jpgm.JPGM_731_17
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