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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Detalles Bibliográficos
Autores principales: Shah, MH, Roshan, R, Desai, R, Kadam, SS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198689/
https://www.ncbi.nlm.nih.gov/pubmed/30147083
http://dx.doi.org/10.4103/jpgm.JPGM_731_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198689/
https://www.ncbi.nlm.nih.gov/pubmed/30147083
http://dx.doi.org/10.4103/jpgm.JPGM_731_17

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