Management of a pregnant patient with chylomicronemia from a novel mutation in GPIHBP1: a case report

BACKGROUND: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive lipid disorder often associated with recurrent episodes of pancreatitis. It is documented in most cases with FCS due to the mutations of key proteins in lipolysis, including LPL, APOC2, APOA5, LMF1 and GPIHBP1. CASE PR...

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Detalles Bibliográficos
Autores principales: Lin, Min-Huan, Tian, Xiao-Hui, Hao, Xiu-Lan, Fei, Hui, Yin, Jian-Lan, Yan, Dan-Dan, Li, Tian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201967/
https://www.ncbi.nlm.nih.gov/pubmed/32375710
http://dx.doi.org/10.1186/s12884-020-02965-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201967/
https://www.ncbi.nlm.nih.gov/pubmed/32375710
http://dx.doi.org/10.1186/s12884-020-02965-1

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