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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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| Foilsithe in: | J Postgrad Med |
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| Main Authors: | , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Medknow Publications & Media Pvt Ltd
2018
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| Ábhair: | |
| Rochtain Ar Líne: | 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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